Medical Device Manufacturer · US , Fort Meyers , FL

Emcyte Corporation

2 submissions · 1 cleared · Since 2019
2
Total
1
Cleared
0
Denied

Emcyte Corporation — FDA 510(k) Submissions

Emcyte Corporation has submitted 2 FDA 510(k) premarket notifications since 2019, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Centrifuges (micro, Ultra, Refrigerated) For Clinical Use, System, Suction, Lipoplasty . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
Filters