Powercrest (M) Sdn. Bhd.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K934546 | POWDER-FREE LATEX EXAMINATION GLOVE | LYY | 1994-01-07 | View |
| 510(k) | K891637 | PATIENT EXAMINATION GLOVES (LATEX) | LYY | 1989-04-14 | View |
No matching devices.
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