Allied Rubber Industries 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) | K896098 | GUARDIAN & JANITEX CONDOM/PROPHYLACTIC | HIS | 1990-12-19 | View |
| 510(k) | K892487 | PATIENT EXAMINATION GLOVES | LYY | 1989-07-14 | View |
No matching devices.
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