510(k) K203141 ยท KNW Instrument, Biopsy
Uramix CuraWay Biopsy Needle
| Applicant | Uramix, Inc., Lansdowne PA, US |
| Decision | Substantially Equivalent, Sep 17, 2021 |
| Received | Oct 20, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203141
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.