What is the U.S. Food and Drug Administration purity standard for medical O2?

	95%
	21%
	90%
	99%

Solutions

Expert Solution

Specificaly the word “purity” it refers to that of how pure of a % of the concentrated oxygen is when it is available to a client who is adminsted to the hospital or any health care setting . According to the U.S food and drug administration the purity of the oxygen that is delivered to the patient should be 99% . That is it should be free from impurities as much as possible

.so option d is the correct answer

This will help to reduce infection occurance in the individual and provide pure O2 for the individual.

Option a, b and c is wrong as the individual will have so much of impurities if it is 95, 21 or 90%

Nightingale answered 1 year ago

Next > < Previous

Related Solutions

2. Consider one of the many dilemmas faced by the U.S. Food and Drug Administration. A...

2. Consider one of the many dilemmas faced by the U.S. Food and Drug Administration. A National Academy of Sciences report estimated that 60,000 women in the United States put their fetuses “at risk” of brain damage from mercury in the fish they ate. FDA scientists have warned that a woman should eat only one can of tuna per week, and that “The action levels we have in place are not protective enough for this—the fetuses.” Nonetheless, after meetings with...

The U.S. Food and Drug Administration (FDA) recently approved the marketing of a new chemical solution,...

The U.S. Food and Drug Administration (FDA) recently approved the marketing of a new chemical solution, Caridex, which disolves cavities. In a study conducted by dental researchers at Northwestern University, 21 of the 35 patients with cavities preffered treatment with Caridex to drilling (Gainesville Sun, Feb. 11, 1988). Find a 90% confidence interval for the true proportion of dental patients who prefer having cavities dissolved with Caridex rather than drilled. (0.46,0.74) (0.44,0.76) (0.39,0.81)

The Food and Drug Administration (FDA) is asked to approve a new drug. The new drug...

The Food and Drug Administration (FDA) is asked to approve a new drug. The new drug should contain less than 25mg of the active ingredient “toxin”, which is assumed to have dangerous side effects. The FDA would like to restrict the error of “approving the drug despite its too high content of toxin” to a maximum risk of 5% (α ≤ 0.05). Let Xi : “ The content of toxin in the i-th pill [in mg].” ∼ N(µ, σ2 )...

A drug company applied for the approval of the Food and Drug Administration (FDA) to market...

A drug company applied for the approval of the Food and Drug Administration (FDA) to market a miracle drug that the company believed could cure some cancers. During the period that the application was under consideration the company's stock rose to $65 per share. The president of the company learned that the FDA application was about to be denied. You are a personal friend of the president, and he told you that he believed that the stock will start trading...

The U.S. Food and Drug Administration (FDA) requires nutrition labeling for most foods. Under FDA regulations,...

The U.S. Food and Drug Administration (FDA) requires nutrition labeling for most foods. Under FDA regulations, manufacturers are required to list the amounts of certain nutrients in their foods, such as calories, sugar, fat, and carbohydrates. This nutritional information is displayed on the food’s package. Calories (C) Sugar (S) Fat (F) Carbohydrates (R) 100 12 0.5 25 130 11 1.5 29 100 1 2 20 130 15 2 31 130 13 1.5 29 120 3 0.5 26 100 2 0...

-Explain standard safety precautions of drug administration. -List and describe the "five rights" of drug administration....

-Explain standard safety precautions of drug administration. -List and describe the "five rights" of drug administration. -Discuss some special patient considerations when administering drugs.

What types of innovative partnerships does the Food and Drug Administration possess that allow it to...

What types of innovative partnerships does the Food and Drug Administration possess that allow it to provide quality public health care? What partnerships could the organization forge to improve the outcomes they can provide?

The Food and Drug Administration will allow a food product to be labeled “sodium free” only...

The Food and Drug Administration will allow a food product to be labeled “sodium free” only if there is strong evidence that it contains, on average, less than 5 milligrams of sodium per serving. A soft drink producer, wishing to use a “salt free” label, has its product tested. A laboratory takes 25 independent sample servings of the soft drink and measures them for sodium content using a technique that is practically free of bias. These measurements average 4.9 milligrams...

What is the definition of a medical device according to the Federal Food, Drug, and Cosmetic...

What is the definition of a medical device according to the Federal Food, Drug, and Cosmetic (FD&C) Act?

1 . The Food and Drug Administration has decided if a particular food product has 8...

1 . The Food and Drug Administration has decided if a particular food product has 8 grams or more of impurities it should be banned. A random sample of 36 cans of Tomato soup produced by Classic Food, Inc. showed 7.4 grams of impurities with a standard deviation of 3 grams. Test the hypothesis at the 1% level of significance. Please show the process of getting the answer 2. A production process is designed to fill cans with exactly 32...

Subjects