Medical Device Manufacturer · US , San Carlos , CA

Rubicor Medical, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2002

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.

Rubicor Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Rubicor Medical, Inc.

8 devices

1-8 of 8

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