Medical Device Manufacturer · US , Washington , DC

Fidia Pharmaceutical Corp. - FDA 510(k) Cleared Devices

10 submissions · 9 cleared · Since 1997

Recent clearances: MODIFICATION OF BIONECT HYDROGEL GAUZE PADS, MODIFICATION OF BIONECT CLEAR HYDROGEL, MODIFICATION OF BIONECT HYDROGEL SPRAY

10

Total

9

Cleared

0

Denied

FDA 510(k) Regulatory Record - Fidia Pharmaceutical Corp. General & Plastic Surgery ✕

10 devices

1-10 of 10

Cleared Feb 10, 1999

MODIFICATION OF BIONECT HYDROGEL GAUZE PADS

General & Plastic Surgery · 85d

Cleared Feb 10, 1999

MODIFICATION OF BIONECT CLEAR HYDROGEL

General & Plastic Surgery · 85d

Cleared Feb 10, 1999

MODIFICATION OF BIONECT HYDROGEL SPRAY

General & Plastic Surgery · 85d

Cleared Feb 10, 1999

MODIFICATION OF BIONECT HYDROGEL FOAM

General & Plastic Surgery · 85d

Cleared Feb 10, 1999

BIONECT HYDROGEL

General & Plastic Surgery · 85d

Cleared Sep 22, 1998

BIONECT HYDROGEL GAUZE PADS

General & Plastic Surgery · 357d

Cleared Sep 22, 1998

BIONECT HYDROGEL FOAM

General & Plastic Surgery · 357d

Cleared Sep 22, 1998

BIONECT HYDROGEL SPRAY

General & Plastic Surgery · 357d

Cleared Sep 22, 1998

BIONECT CLEAR HYDROGEL

General & Plastic Surgery · 357d

Cleared Feb 12, 1997

General & Plastic Surgery · 194d