Arent Fox
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K945843 | SAFETY PLUS | EJI | 1995-07-11 | View |
| 510(k) | K944053 | NATURAL RUBBER LATEX SURGEONS GLOVE | KGO | 1995-04-25 | View |
| 510(k) | K945583 | OCUSYSTEM(ART) | HQC | 1995-02-13 | View |
| 510(k) | K944054 | POWDER FREE SURGEON'S GLOVE | KGD | 1994-11-17 | View |
No matching devices.
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