Sanarus Medical, Inc.

14 FDA 510(k) clearances · Manufacturer

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Record	Firm	Date
SANARUS INCORE ROTATIONAL CORE BIOPSY DEVICE, MODELS CB3010, CB3012 (K080171)	Sanarus Medical, Inc.	2008-03-06
SANARUS V2 TREATMENT SYSTEM (K073533)	Sanarus Medical, Inc.	2008-02-07
V2 TREATMENT SYSTEM (V2 CONSOLE, V2 ICE PROBE, V2 DEWARS) MODELS; VS3000, VP0600, VD0600 (K062896)	Sanarus Medical, Inc.	2007-01-03
SANARUS VISICA TREATMENT SYSTEM (K061510)	Sanarus Medical, Inc.	2006-07-18
MODIFICATION TO:SANARUS VISICA TREATMENT SYSTEM , MODELS VS2000 (K052861)	Sanarus Medical, Inc.	2005-11-15
SANARUS CASSI II ROTATIONAL CORE BIOPSY SYSTEM, MODEL CS2000 (K051581)	Sanarus Medical, Inc.	2005-07-27
SANARUS CASSI ROTATIONAL CORE BIOPSY SYSTEM (K042136)	Sanarus Medical, Inc.	2004-09-08
SANARUS CENTRICA II ROTATIONAL CORE BIOPSY SYSTEM (K032506)	Sanarus Medical, Inc.	2003-10-09
SANARUS INDICA MARKER SYSTEM (K020054)	Sanarus Medical, Inc.	2002-10-16
SANARUS VISICA TREATMENT SYSTEM (K022314)	Sanarus Medical, Inc.	2002-10-15
MODIFICATION TO SANARUS CENTRICA CORE TISSUE BIOPSY (K022879)	Sanarus Medical, Inc.	2002-09-23
SANARUS CENTRICA CORE TISSUE BIOPSY SYSTEM (K021137)	Sanarus Medical, Inc.	2002-06-26
MODIFICATION TO SANARUS VISICA TREATMENT SYSTEM (K021211)	Sanarus Medical, Inc.	2002-06-26
SANARUS VISICA TREATMENT SYSTEM (K020605)	Sanarus Medical, Inc.	2002-03-08

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