Dmp, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K892965 | LATEX EXAM GLOVES (MFG. BROADLAND RUBBER INDUST.) | LYY | 1989-06-14 | View |
| 510(k) | K892150 | PATIENT EXAMINATION GLOVES (LATEX) | LYY | 1989-06-06 | View |
| 510(k) | K891661 | PATIENT EXAMINATION GLOVES (LATEX) | LYY | 1989-05-25 | View |
No matching devices.
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