21 C.F.R. § 814.19
Current through November 30, 2024
A class III device for which a product development protocol has been declared completed by FDA under this chapter will be considered to have an approved PMA.
21 C.F.R. §814.19
A class III device for which a product development protocol has been declared completed by FDA under this chapter will be considered to have an approved PMA.
21 C.F.R. §814.19