Allied Biomedical Corp.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K982051 | KELOCATE SHEETING | MDA | 1998-08-05 | View |
| 510(k) | K971479 | DURALASTIC ANATOMICAL MALAR IMPLANTS | LZK | 1997-07-18 | View |
| 510(k) | K971481 | DURALASTIC ANATOMICAL NASAL IMPLANTS | FZE | 1997-07-18 | View |
| 510(k) | K971478 | DURALASTIC ANATOMICAL CHIN IMPLANTS | FWP | 1997-07-18 | View |
| 510(k) | K971480 | DURALASTIC I AND DURALASTIC II | MIB | 1997-05-28 | View |
| 510(k) | K955368 | DURALASTIC I | MIB | 1996-02-08 | View |
| 510(k) | K955370 | DURALASTIC II | MIB | 1996-02-08 | View |
| 510(k) | K955433 | DURALASTIC SILICONE TUBING | KGZ | 1996-01-26 | View |
| 510(k) | K954413 | KELOCOTE | MDA | 1995-11-29 | View |
No matching devices.
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