Sanarus Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sanarus Medical, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Sanarus Medical, Inc. has 14 FDA 510(k) cleared medical devices. Based in Pleasanton, US.
Historical record: 14 cleared submissions from 2002 to 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Sanarus Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sanarus Medical, Inc.
14 devices
Cleared
Mar 06, 2008
SANARUS INCORE ROTATIONAL CORE BIOPSY DEVICE, MODELS CB3010, CB3012
Gastroenterology & Urology
42d
Cleared
Feb 07, 2008
SANARUS V2 TREATMENT SYSTEM
General & Plastic Surgery
52d
Cleared
Jan 03, 2007
V2 TREATMENT SYSTEM (V2 CONSOLE, V2 ICE PROBE, V2 DEWARS) MODELS
General & Plastic Surgery
98d
Cleared
Jul 18, 2006
SANARUS VISICA TREATMENT SYSTEM
General & Plastic Surgery
47d
Cleared
Nov 15, 2005
MODIFICATION TO:SANARUS VISICA TREATMENT SYSTEM , MODELS VS2000
General & Plastic Surgery
35d
Cleared
Jul 27, 2005
SANARUS CASSI II ROTATIONAL CORE BIOPSY SYSTEM, MODEL CS2000
Gastroenterology & Urology
42d
Cleared
Sep 08, 2004
SANARUS CASSI ROTATIONAL CORE BIOPSY SYSTEM
Gastroenterology & Urology
30d
Cleared
Oct 09, 2003
SANARUS CENTRICA II ROTATIONAL CORE BIOPSY SYSTEM
Gastroenterology & Urology
56d
Cleared
Oct 16, 2002
SANARUS INDICA MARKER SYSTEM
General & Plastic Surgery
281d
Cleared
Oct 15, 2002
SANARUS VISICA TREATMENT SYSTEM
General & Plastic Surgery
90d
Cleared
Sep 23, 2002
MODIFICATION TO SANARUS CENTRICA CORE TISSUE BIOPSY
Gastroenterology & Urology
24d
Cleared
Jun 26, 2002
SANARUS CENTRICA CORE TISSUE BIOPSY SYSTEM
Gastroenterology & Urology
78d