The Safe Medical Devices Act, 1990 requires
a. that injuries, illness, or death from any device be reported.
b. premarket approval of devices.
c. safety testing of devices before and after they have been marketed
d. that all problems and potential problems be reported to the FDA.
a
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Pharmacies and ________ equipment (DME) companies can be more flexible than providers' offices in their requirements for authorizations for the release of information.
Fill in the blank(s) with the appropriate word(s).
____________________ is the absence of a pulse with organized activity on cardiac monitoring.
Fill in the blank(s) with the appropriate word(s).
Which of the following sets is expected to become a future measure set?
A) Venous thromboembolism B) Nursing sensitive care C) Stroke D) None of the above E) All of the above
Which paper form was designed for institutional claims?
What will be an ideal response?