Invatec S.P.A.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K100921 | ADMIRAL XTREME PTA BALLOON DILATATION CATHETER | LIT | 2010-04-30 | View |
| 510(k) | K092352 | SCUBA BILIARY STENT SYSTEM | FGE | 2010-03-16 | View |
| 510(k) | K092361 | REEF HP 0.035 OTW PTA BALLOON DILATATION CATHETER | LIT | 2009-10-29 | View |
| 510(k) | K092177 | MO.MA ULTRA PROXIMAL CEREBRAL PROTECTION DEVICE, MODEL MUS0130069X6 | NTE | 2009-10-15 | View |
No matching devices.
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