Medical Device Manufacturer · US , Suunyvale , CA

Perkinelmer Optoelectronics

2 submissions · 2 cleared · Since 1991
2
Total
2
Cleared
0
Denied

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.

2 devices
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