Angiologica B. M. Srl
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) | K090432 | HEMORPEX SYSTEM | FER | 2009-05-29 | View |
| 510(k) | K043191 | REPOL ANGIMESH, ANGIMESH PRE, FOLDED MESH, REPOL PLUG BASIC, REPOL PLUG CAP, REPOL PLUG FLOWER AND WINGS MESH | FTL | 2005-05-16 | View |
No matching devices.
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