Sanarus Medical, Inc.
Sanarus Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2008.
Top product codes for Sanarus Medical, Inc.
Recent clearances by Sanarus Medical, Inc.
- K080171 — SANARUS INCORE ROTATIONAL CORE BIOPSY DEVICE, MODELS CB3010, CB3012
- K073533 — SANARUS V2 TREATMENT SYSTEM
- K062896 — V2 TREATMENT SYSTEM (V2 CONSOLE, V2 ICE PROBE, V2 DEWARS) MODELS; VS3000, VP0600, VD0600
- K061510 — SANARUS VISICA TREATMENT SYSTEM
- K052861 — MODIFICATION TO:SANARUS VISICA TREATMENT SYSTEM , MODELS VS2000
- K051581 — SANARUS CASSI II ROTATIONAL CORE BIOPSY SYSTEM, MODEL CS2000
- K042136 — SANARUS CASSI ROTATIONAL CORE BIOPSY SYSTEM
- K032506 — SANARUS CENTRICA II ROTATIONAL CORE BIOPSY SYSTEM
- K020054 — SANARUS INDICA MARKER SYSTEM
- K022314 — SANARUS VISICA TREATMENT SYSTEM
- K022879 — MODIFICATION TO SANARUS CENTRICA CORE TISSUE BIOPSY
- K021137 — SANARUS CENTRICA CORE TISSUE BIOPSY SYSTEM
- K021211 — MODIFICATION TO SANARUS VISICA TREATMENT SYSTEM
- K020605 — SANARUS VISICA TREATMENT SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.