Rubicor Medical, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
FDA 510(k) Regulatory Record - Rubicor Medical, Inc. General & Plastic Surgery ✕
6 devices
Cleared
Mar 09, 2007
FLEXIBLE LOOP ELECTROSURGICAL ELECTRODE
General & Plastic Surgery
39d
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