CFR 21-814.20-2013
Food and Drugs. Part814:Premarket approval of medical devices. Section814.20:Application.

Standard No.

CFR 21-814.20-2013

Release Date

2013

Published By

US-CFR-file

Latest

CFR 21-814.20-2013

Scope

(a) The applicant or an authorized representative shall sign the PMA. If the applicant does not reside or have a place of business within the United States, the PMA shall be countersigned by an authorized representative residing or maintaining a place of

CFR 21-814.20-2013 history

• 2013 CFR 21-814.20-2013 Food and Drugs. Part814:Premarket approval of medical devices. Section814.20:Application.