Spiration, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories3
Latest FDA decision2017-11-20
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K171492 | B7 2C Occlusion Balloon | EOQ | 2017-11-20 | View |
| 510(k) | K170990 | Active Needle Endoscopic Treatment (ANET) Electrosurgical Applicator | GEI | 2017-05-11 | View |
| 510(k) | K162611 | PeriFLEX | EOQ | 2017-02-09 | View |
| 510(k) | K152922 | ViziShot FLEX | KTI | 2016-02-19 | View |
No matching devices.