Assurguard 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) | K123757 | POWDER FREE LATEX PATIENT EXAMINATION GLOVES, WITH PROTEIN CONTENT LABELING CLAIM, NATURAL COLOR | LYY | 2013-02-01 | View |
| 510(k) | K123760 | MULTIPLE NAME | LZA | 2013-01-28 | View |
No matching devices.
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