Rubberex (M) Sdn Berhad
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) | K893782 | PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER | LYY | 1989-07-14 | View |
| 510(k) | K891389 | PATIENT EXAMINATION GLOVES (LATEX) | LYY | 1989-05-12 | View |
No matching devices.
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