Glove Seal Sdn Bhd
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K983570 | GLOVE SEAL D'PRO LATEX EXAMINATION GLOVE | LYY | 1999-01-14 | View |
| 510(k) | K891147 | PATIENT EXAMINATION GLOVE (LATEX) | LYY | 1989-04-28 | View |
No matching devices.