Medical Device Manufacturer · US , Melbourne , FL

Slater Endoscopy, LLC

3 submissions · 3 cleared · Since 2014
3
Total
3
Cleared
0
Denied

Slater Endoscopy, LLC — FDA 510(k) Submissions

Slater Endoscopy, LLC has submitted 3 FDA 510(k) premarket notifications since 2014, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Endoscopic Grasping/cutting Instrument, Non-powered, Forceps, Biopsy, Electric . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
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All3 Gastroenterology & Urology 3