Medical Device Manufacturer · US , Silver Spring , MD

American Fluoroseal Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1987

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - American Fluoroseal Corp. Pathology ✕

2 devices

1-2 of 2

Cleared Mar 30, 1994

KAPTON PEEL POUCH

Pathology · 271d

Cleared Mar 30, 1987

TISSUE CULTURE BAG

Pathology · 27d