Propper Manufacturing Co., Inc.

Propper Manufacturing Co., Inc. — FDA 510(k) Submissions

Propper Manufacturing Co., Inc. has submitted 7 FDA 510(k) premarket notifications since 2014, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Indicator, Physical/chemical Sterilization Process, Ophthalmoscope, Ac-powered, Wrap, Sterilization . Use the specialty filter in the sidebar to narrow results.