Sentreheart, 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) | K090385 | LARIAT II SUTURE DELIVERY DEVICE | GAT | 2009-05-06 | View |
| 510(k) | K080364 | FINDRWIRZ GUIDE WIRE SYSTEM | DQX | 2008-08-11 | View |
| 510(k) | K070126 | OCCLUSION BALLOON CATHETER | DQY | 2008-02-08 | View |
No matching devices.
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