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Sanarus Medical, Inc.

FDA 510(k) & PMA Approved Devices — 14 products

Total Devices14
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K080171 SANARUS INCORE ROTATIONAL CORE BIOPSY DEVICE, MODELS CB3010, CB3012KNW2008-03-06 View
510(k) K073533 SANARUS V2 TREATMENT SYSTEMGEH2008-02-07 View
510(k) K062896 V2 TREATMENT SYSTEM (V2 CONSOLE, V2 ICE PROBE, V2 DEWARS) MODELS; VS3000, VP0600, VD0600GEH2007-01-03 View
510(k) K061510 SANARUS VISICA TREATMENT SYSTEMGEH2006-07-18 View
510(k) K052861 MODIFICATION TO:SANARUS VISICA TREATMENT SYSTEM , MODELS VS2000GEH2005-11-15 View
510(k) K051581 SANARUS CASSI II ROTATIONAL CORE BIOPSY SYSTEM, MODEL CS2000KNW2005-07-27 View
510(k) K042136 SANARUS CASSI ROTATIONAL CORE BIOPSY SYSTEMKNW2004-09-08 View
510(k) K032506 SANARUS CENTRICA II ROTATIONAL CORE BIOPSY SYSTEMKNW2003-10-09 View
510(k) K020054 SANARUS INDICA MARKER SYSTEMFZP2002-10-16 View
510(k) K022314 SANARUS VISICA TREATMENT SYSTEMGEH2002-10-15 View
510(k) K022879 MODIFICATION TO SANARUS CENTRICA CORE TISSUE BIOPSYKNW2002-09-23 View
510(k) K021137 SANARUS CENTRICA CORE TISSUE BIOPSY SYSTEMKNW2002-06-26 View
510(k) K021211 MODIFICATION TO SANARUS VISICA TREATMENT SYSTEMGEH2002-06-26 View
510(k) K020605 SANARUS VISICA TREATMENT SYSTEMGEH2002-03-08 View
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