Company ยท US
Fidia Pharmaceutical Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1997 to 1999. Name variants (Inc, Corp, punctuation) are merged.
10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| MGQ | Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic | 10 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Feb 10, 1999 | K984413 | BIONECT HYDROGEL Fidia Pharmaceutical Corp. | MGQ |
| Feb 10, 1999 | K984267 | MODIFICATION OF BIONECT HYDROGEL FOAM Fidia Pharmaceutical Corp. | MGQ |
| Feb 10, 1999 | K984266 | MODIFICATION OF BIONECT HYDROGEL SPRAY Fidia Pharmaceutical Corp. | MGQ |
| Feb 10, 1999 | K984264 | MODIFICATION OF BIONECT CLEAR HYDROGEL Fidia Pharmaceutical Corp. | MGQ |
| Feb 10, 1999 | K984262 | MODIFICATION OF BIONECT HYDROGEL GAUZE PADS Fidia Pharmaceutical Corp. | MGQ |
| Sep 22, 1998 | K973725 | BIONECT CLEAR HYDROGEL Fidia Pharmaceutical Corp. | MGQ |
| Sep 22, 1998 | K973724 | BIONECT HYDROGEL SPRAY Fidia Pharmaceutical Corp. | MGQ |
| Sep 22, 1998 | K973722 | BIONECT HYDROGEL FOAM Fidia Pharmaceutical Corp. | MGQ |
| Sep 22, 1998 | K973721 | BIONECT HYDROGEL GAUZE PADS Fidia Pharmaceutical Corp. | MGQ |
| Feb 12, 1997 | K963004 | BIONECT CREAM Fidia Pharmaceutical Corp. | MGQ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||