Teleflex, Inc.
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest FDA decision2016-06-21
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K153652 | ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set | CAZ | 2016-06-21 | View |
No matching devices.
Related Clinical Trials
NCT06604039A Clinical Registry to Demonstrate the Safety and Performance of Teleflex Vascular Access DevicesRECRUITINGNCT06779630Safety and Effectiveness of the Orsiro Mission 48-mm Sirolimus Eluting Coronary Stent System in Subjects With Coronary Artery LesionsRECRUITINGNCT07258290Safety and Clinical Performance of the Freesolve Resorbable Magnesium Scaffold (RMS) System in Subjects With Coronary Artery LesionsRECRUITINGNCT07782762Effectiveness of the NowCath Foley in Reducing Catheter-Associated UTIs and Blockages in Long-Term Indwelling Catheter Users (REDUCE)RECRUITING