Surefire Medical, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K180677 | Surefire Spark Infusion System | DQO | 2018-04-03 | View |
| 510(k) | K171355 | Surefire Precision Infusion System | DQO | 2017-05-17 | View |
| 510(k) | K162359 | Surefire Guiding Catheter | DQY | 2016-09-21 | View |
| 510(k) | K160662 | Surefire Infusion System | DQO | 2016-03-11 | View |
| 510(k) | K122506 | SUREFIRE HIGH FLOW ANGIOGRAPHIC CATHETER, ACCESS | DQX | 2012-09-17 | View |
| 510(k) | K121677 | SUREFIRE HI-FLOW MICROCATHETER | DQO | 2012-06-14 | View |
| 510(k) | K113737 | SUREFIRE GUIDE SHEATH | DQO | 2012-02-23 | View |
| 510(k) | K110459 | SUREFIRE INFUSION CATHETER SYSTEM | DQO | 2011-06-24 | View |
No matching devices.
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