510(k) K220595 ยท KNW Instrument, Biopsy
NeoNavia Biopsy System
| Applicant | Neodynamics AB, Lidingo, SE |
| Decision | Substantially Equivalent, Sep 8, 2022 |
| Received | Mar 1, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220595
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.