Medical Device Manufacturer · US , Lewisberry , PA

Dimesol, Inc.

2 submissions · 2 cleared · Since 2018
2
Total
2
Cleared
0
Denied

Dimesol, Inc. — FDA 510(k) Submissions

Dimesol, Inc. has submitted 2 FDA 510(k) premarket notifications since 2018, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Needle, Fistula, Set, Tubing, Blood, With And Without Anti-regurgitation Valve . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Gastroenterology & Urology 2