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

American Fluoroseal Corp. has 2 FDA 510(k) cleared medical devices. Based in Silver Spring, US.

Historical record: 2 cleared submissions from 1987 to 1994. Primary specialty: Pathology.

Browse the FDA 510(k) cleared devices submitted by American Fluoroseal Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - American Fluoroseal Corp.
2 devices
1-2 of 2
Cleared Mar 30, 1994
KAPTON PEEL POUCH
K933228 · KJA
Pathology · 271d
Cleared Mar 30, 1987
TISSUE CULTURE BAG
K870865 · KJA
Pathology · 27d
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