Sanarus Medical, Inc.
FDA 510(k) medical device clearances.
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.