R4 Vascular, Inc.
R4 Vascular, Inc. holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2013.
Top product codes for R4 Vascular, Inc.
Recent clearances by R4 Vascular, Inc.
- K131329 — VECTOR PTA BALLOON DILATATION CATHETER
- K121385 — VECTOR
- K100169 — DURASPAN HEMODIALYSIS LONG-TERM CATHETER
- K091506 — DURASPAN HEMODIALYSIS LONG-TERM CATHETER, MODELS 62152420, 621512820, 62153220, 62153620, 62154020, 62155520
- K092040 — PHEROCIOUS 10.5 FR (24 CM, 28 CM AND 32 CM), MODELS 430102440, 430102840, 430103240
- K083763 — ZEUS CT PICC 4 FR AND 5 FR SINGLE AND DUAL LUMEN
- K071361 — R4 VASCULAR INC. PEGASUS CT PICC, MODEL 500005-001,002, 004, 005, 500004-001, 002,004,005
Data sourced from openFDA. This site is unofficial and independent of the FDA.