FDA 510(k) Applications Submitted by R4 VASCULAR, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K100169 |
01/20/2010 |
DURASPAN HEMODIALYSIS LONG-TERM CATHETER |
R4 VASCULAR, INC. |
| K131329 |
05/08/2013 |
VECTOR PTA BALLOON DILATATION CATHETER |
R4 VASCULAR, INC. |
| K091506 |
05/21/2009 |
DURASPAN HEMODIALYSIS LONG-TERM CATHETER, MODELS 62152420, 621512820, 62153220, 62153620, 62154020, 62155520 |
R4 VASCULAR, INC. |
| K092040 |
07/02/2009 |
PHEROCIOUS 10.5 FR (24 CM, 28 CM AND 32 CM), MODELS 430102440, 430102840, 430103240 |
R4 VASCULAR, INC. |
| K083763 |
12/18/2008 |
ZEUS CT PICC 4 FR AND 5 FR SINGLE AND DUAL LUMEN |
R4 VASCULAR, INC. |
| K121385 |
05/08/2012 |
VECTOR |
R4 VASCULAR, INC. |
| K071361 |
05/15/2007 |
R4 VASCULAR INC. PEGASUS CT PICC, MODEL 500005-001,002, 004, 005, 500004-001, 002,004,005 |
R4 VASCULAR, INC. |
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