510(k) K012023 ยท KNW Instrument, Biopsy
ANCHOR GUIDE LESION LOCALIZATION DEVICE; ANCOR GUIDE HOLDER; RF GENERATOR CABLE
| Applicant | Senorx, Inc., Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Sep 12, 2001 |
| Received | Jun 28, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012023
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.