Cardiosolutions, 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) | K131332 | CARDIOSOLUTIONS PERCU-PRO STEERABLE INTRODUCER | DYB | 2013-07-19 | View |
| 510(k) | K094048 | PERCUPRO MESSENGER BALLOON CATHETER | DYG | 2011-07-14 | View |
| 510(k) | K094062 | PERCU-PRO GUIDEWIRE | DQX | 2010-09-27 | View |
No matching devices.
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