Arrow International, LLC (A subsidiary of Teleflex, Inc.)
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories3
Latest FDA decision2025-03-14
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K243599 | Arrow™ Endurance™ Extended Dwell Peripheral Catheter System (EDC-00818) | FOZ | 2025-03-14 | View |
| 510(k) | K242281 | Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00620); Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00622); Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00820); Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00822) | FOZ | 2024-12-20 | View |
| 510(k) | K220280 | Arrow Stiffening Stylet | DRB | 2022-08-30 | View |
| 510(k) | K220363 | VPS Rhythm DLX Device with TipTracker Technology | LJS | 2022-08-22 | View |
No matching devices.