Medical Device Manufacturer · US , Silver Spring , MD

American Fluoroseal Corp.

2 submissions · 2 cleared · Since 1987
2
Total
2
Cleared
0
Denied

American Fluoroseal Corp. — FDA 510(k) Submissions

American Fluoroseal Corp. has submitted 2 FDA 510(k) premarket notifications since 1987, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Flask, Tissue Culture . Use the specialty filter in the sidebar to narrow results.

2 devices
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