21 CFR § 814.19 Premarket Approval of Medical Devices

§ 814.19 Product development protocol (PDP).

Current through Sep 8, 2026 · Read all of Part 814

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.

← § 814.17 Service of orders.§ 814.20 Application. →