Rubicor Medical, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K071048 | RUBICOR MAGIC BREAST BIOPSY DEVICE, MODEL 31537 | KNW | 2007-05-15 | View |
| 510(k) | K070275 | FLEXIBLE LOOP ELECTROSURGICAL ELECTRODE | GEI | 2007-03-09 | View |
| 510(k) | K053151 | RUBICOR MAGIC BREAST BIOPSY DEVICE | KNW | 2005-11-18 | View |
| 510(k) | K052506 | RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 31108 | GEI | 2005-10-06 | View |
| 510(k) | K032584 | RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30629 | GEI | 2003-09-17 | View |
| 510(k) | K030049 | MODIFICATION TO RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30086 | GEI | 2003-01-29 | View |
| 510(k) | K023601 | RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30086 | GEI | 2002-11-19 | View |
| 510(k) | K020047 | RUBICOR BREAST BIOPSY DEVICE | GEI | 2002-04-05 | View |
No matching devices.
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