Rubicor Medical, Inc.
FDA 510(k) medical device clearances.
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.