Company ยท US
Allied Biomedical Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 1998. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 5, 1998 | K982051 | KELOCATE SHEETING Allied Biomedical Corp. | MDA |
| Jul 18, 1997 | K971481 | DURALASTIC ANATOMICAL NASAL IMPLANTS Allied Biomedical Corp. | FZE |
| Jul 18, 1997 | K971479 | DURALASTIC ANATOMICAL MALAR IMPLANTS Allied Biomedical Corp. | LZK |
| Jul 18, 1997 | K971478 | DURALASTIC ANATOMICAL CHIN IMPLANTS Allied Biomedical Corp. | FWP |
| May 28, 1997 | K971480 | DURALASTIC I AND DURALASTIC II Allied Biomedical Corp. | MIB |
| Feb 8, 1996 | K955370 | DURALASTIC II Allied Biomedical Corp. | MIB |
| Feb 8, 1996 | K955368 | DURALASTIC I Allied Biomedical Corp. | MIB |
| Jan 26, 1996 | K955433 | DURALASTIC SILICONE TUBING Allied Biomedical Corp. | KGZ |
| Nov 29, 1995 | K954413 | KELOCOTE Allied Biomedical Corp. | MDA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||