Mmi, 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) | K905026 | DUAL FLEX NON-LATEX | FGD | 1991-12-18 | View |
| 510(k) | K860445 | CLAMP-N-CUT | HFW | 1986-04-04 | View |
| 510(k) | K842130 | G.I. CLEANSING KIT | FCE | 1984-08-08 | View |
No matching devices.
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