Sanarus Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SANARUS INCORE ROTATIONAL CORE BIOPSY DEVICE, MODELS CB3010, CB3012, SANARUS V2 TREATMENT SYSTEM, V2 TREATMENT SYSTEM (V2 CONSOLE, V2 ICE PROBE, V2 DEWARS) MODELS
14
Total
14
Cleared
0
Denied
FDA 510(k) Regulatory Record - Sanarus Medical, Inc. Gastroenterology & Urology ✕
6 devices
Cleared
Mar 06, 2008
SANARUS INCORE ROTATIONAL CORE BIOPSY DEVICE, MODELS CB3010, CB3012
Gastroenterology & Urology
42d
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
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