Darchet (Usa), Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K891663 | LEEDAR (PATIENT EXAMINATION GLOVES - LATEX) | LYY | 1990-02-13 | View |
| 510(k) | K891662 | PATIENT EXAMINATION GLOVES (LATEX) | LYY | 1990-01-26 | View |
No matching devices.
Advertisement