R4 Vascular, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
Advertisement
Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K131329 | VECTOR PTA BALLOON DILATATION CATHETER | LIT | 2013-06-06 | View |
| 510(k) | K121385 | VECTOR | LIT | 2012-06-14 | View |
| 510(k) | K100169 | DURASPAN HEMODIALYSIS LONG-TERM CATHETER | MSD | 2010-02-18 | View |
| 510(k) | K091506 | DURASPAN HEMODIALYSIS LONG-TERM CATHETER, MODELS 62152420, 621512820, 62153220, 62153620, 62154020, 62155520 | MSD | 2010-01-08 | View |
| 510(k) | K092040 | PHEROCIOUS 10.5 FR (24 CM, 28 CM AND 32 CM), MODELS 430102440, 430102840, 430103240 | LJS | 2009-11-18 | View |
| 510(k) | K083763 | ZEUS CT PICC 4 FR AND 5 FR SINGLE AND DUAL LUMEN | LJS | 2009-03-16 | View |
| 510(k) | K071361 | R4 VASCULAR INC. PEGASUS CT PICC, MODEL 500005-001,002, 004, 005, 500004-001, 002,004,005 | LJS | 2007-08-20 | View |
No matching devices.
Advertisement