510(k) K180233 ยท KNW Instrument, Biopsy
Eviva Stereotactic Guided Breast Biopsy System
| Applicant | Hologic, Inc., Malborough MA, US |
| Decision | Substantially Equivalent, Apr 10, 2018 |
| Received | Jan 29, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180233
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.