510(k) K003439 ยท KNW Instrument, Biopsy
VIVANT BREAST LESION LOCALIZATION DEVICE
| Applicant | Vivant Medical, Inc., Portola Valley CA, US |
| Decision | Substantially Equivalent, Dec 15, 2000 |
| Received | Nov 6, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003439
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.