Medical Device Manufacturer · US , Germantown , MD

Medispec, Ltd.

4 submissions · 4 cleared · Since 1998
4
Total
4
Cleared
0
Denied

Medispec, Ltd. — FDA 510(k) Submissions

Medispec, Ltd. has submitted 4 FDA 510(k) premarket notifications since 1998, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Lithotriptor, Extracorporeal Shock-wave, Urological, Massager, Therapeutic, Electric, Lithotriptor, Electro-hydraulic . Use the specialty filter in the sidebar to narrow results.

4 devices
1–4 of 4
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All4 Gastroenterology & Urology 3 Physical Medicine 1