510(k) K053151 ยท KNW Instrument, Biopsy
RUBICOR MAGIC BREAST BIOPSY DEVICE
| Applicant | Rubicor Medical, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Nov 18, 2005 |
| Received | Nov 10, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053151
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.