Rubicor Medical, Inc.
Rubicor Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2007.
Top product codes for Rubicor Medical, Inc.
Recent clearances by Rubicor Medical, Inc.
- K071048 — RUBICOR MAGIC BREAST BIOPSY DEVICE, MODEL 31537
- K070275 — FLEXIBLE LOOP ELECTROSURGICAL ELECTRODE
- K053151 — RUBICOR MAGIC BREAST BIOPSY DEVICE
- K052506 — RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 31108
- K032584 — RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30629
- K030049 — MODIFICATION TO RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30086
- K023601 — RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30086
- K020047 — RUBICOR BREAST BIOPSY DEVICE
Data sourced from openFDA. This site is unofficial and independent of the FDA.