Medical Device Manufacturer · US , Washington , DC

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

10 submissions · 9 cleared · Since 1997

Total

Cleared

Denied

Fidia Pharmaceutical Corp. has 9 FDA 510(k) cleared general & plastic surgery devices. Based in Washington, US.

Historical record: 9 cleared submissions from 1997 to 1999.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

Fidia Pharmaceutical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Fidia Pharmaceutical Corp.

10 devices

1-10 of 10

Cleared Feb 10, 1999

MODIFICATION OF BIONECT HYDROGEL GAUZE PADS

K984262 · MGQ

General & Plastic Surgery · 85d

Cleared Feb 10, 1999

MODIFICATION OF BIONECT CLEAR HYDROGEL

K984264 · MGQ

General & Plastic Surgery · 85d

Cleared Feb 10, 1999

MODIFICATION OF BIONECT HYDROGEL SPRAY

K984266 · MGQ

General & Plastic Surgery · 85d

Cleared Feb 10, 1999

MODIFICATION OF BIONECT HYDROGEL FOAM

K984267 · MGQ

General & Plastic Surgery · 85d

Cleared Feb 10, 1999

BIONECT HYDROGEL

K984413 · MGQ

General & Plastic Surgery · 85d

Cleared Sep 22, 1998

BIONECT HYDROGEL GAUZE PADS

K973721 · MGQ

General & Plastic Surgery · 357d

Cleared Sep 22, 1998

BIONECT HYDROGEL FOAM

K973722 · MGQ

General & Plastic Surgery · 357d

Cleared Sep 22, 1998

BIONECT HYDROGEL SPRAY

K973724 · MGQ

General & Plastic Surgery · 357d

Cleared Sep 22, 1998

BIONECT CLEAR HYDROGEL

K973725 · MGQ

General & Plastic Surgery · 357d

Cleared Feb 12, 1997

BIONECT CREAM

K963004 · MGQ

General & Plastic Surgery · 194d

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

FDA 510(k) Regulatory Record - Fidia Pharmaceutical Corp.

Filters