Rhythm Xience, Inc. (Rxi)
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2017-05-09
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K171081 | Guider Catheter Introducer | DYB | 2017-05-09 | View |
| 510(k) | K170373 | Flextra Steerable Introducer | DYB | 2017-02-27 | View |
No matching devices.