Rubicor Medical, Inc. is one of 15067 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rubicor Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: RUBICOR MAGIC BREAST BIOPSY DEVICE, MODEL 31537, FLEXIBLE LOOP ELECTROSURGICAL ELECTRODE, RUBICOR MAGIC BREAST BIOPSY DEVICE
8
Total
8
Cleared
0
Denied
Rubicor Medical, Inc. has 8 FDA 510(k) cleared medical devices. Based in San Carlos, US.
Historical record: 8 cleared submissions from 2002 to 2007. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Rubicor Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Rubicor Medical, Inc.
8 devices
Cleared
May 15, 2007
RUBICOR MAGIC BREAST BIOPSY DEVICE, MODEL 31537
Gastroenterology & Urology
32d
Cleared
Mar 09, 2007
FLEXIBLE LOOP ELECTROSURGICAL ELECTRODE
General & Plastic Surgery
39d
Cleared
Nov 18, 2005
RUBICOR MAGIC BREAST BIOPSY DEVICE
Gastroenterology & Urology
8d
Cleared
Oct 06, 2005
RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 31108
General & Plastic Surgery
23d
Cleared
Sep 17, 2003
RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30629
General & Plastic Surgery
27d
Cleared
Jan 29, 2003
MODIFICATION TO RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30086
General & Plastic Surgery
23d
Cleared
Nov 19, 2002
RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30086
General & Plastic Surgery
22d
Cleared
Apr 05, 2002
RUBICOR BREAST BIOPSY DEVICE
General & Plastic Surgery
88d