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  2. Investigational device exemption - Wikipedia

    en.wikipedia.org/wiki/Investigational_Device...

    An investigational device exemption (IDE) allows an investigational device (i.e. a device that is the subject of a clinical study [1]) to be used in order to collect safety and effectiveness data required to support a premarket approval (PMA) application or a premarket notification [510(k)] submission to Food and Drug Administration (FDA). [2]

  3. Substantial equivalence - Wikipedia

    en.wikipedia.org/wiki/Substantial_equivalence

    The term was borrowed from the FDA's 1976 substantial equivalence definition for new medical devices—under Premarket Notification 510(k), a new Class II device that is essentially similar to an existing device can be cleared for release without further testing.

  4. Federal Food, Drug, and Cosmetic Act of 1938 - Wikipedia

    en.wikipedia.org/wiki/Federal_Food,_Drug,_and...

    Section 510(k) [28] of the Federal Food, Drug, and Cosmetic Act requires those device manufacturers who must register to notify FDA, at least 90 days in advance, of their intent to market a medical device. This is known as premarket notification, PMN, or 510(k).

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  6. Template:AfC submission/draftnew - Wikipedia

    en.wikipedia.org/wiki/Template:AFC_submission/...

    This template is meant as a single template for marking the status of an Articles for creation submission. To use this template to submit an article for review, use {{subst:submit|username}}, where username is the username of the draft's creator (left blank it will assume it is you). The template uses one of the following parameter options:

  7. Medical textiles - Wikipedia

    en.wikipedia.org/wiki/Medical_textiles

    [64] 510(K) is a premarket submission made to the Food and Drug Administration in order to demonstrate that the device to be sold is safe and effective. Surgical and surgical isolation gowns are regulated by the FDA as Class II medical devices that require a 510(k). Non-surgical gowns are class I medical devices that do not need a 510(k) clearance.

  8. Template:AfC submission/message - Wikipedia

    en.wikipedia.org/wiki/Template:AFC_submission/...

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Donate

  9. National Donor Deferral Registry - Wikipedia

    en.wikipedia.org/wiki/National_Donor_Deferral...

    The National Donor Deferral Registry, also known as the (NDDR) is a database of individuals who have tested "reactive" for viral agents like human immunodeficiency viruses (HIV), Hepatitis B virus (HBV), and hepatitis C virus (HCV) and are permanently prohibited from donating plasma. [1]