Perkinelmer Optoelectronics

Perkinelmer Optoelectronics — FDA 510(k) Submissions

Perkinelmer Optoelectronics has submitted 2 FDA 510(k) premarket notifications since 1991, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Light Source, Endoscope, Xenon Arc, Light, Surgical, Floor Standing . Use the specialty filter in the sidebar to narrow results.