510(k) K193268 ยท KNW Instrument, Biopsy
APrioCore Plus
| Applicant | Apriomed AB, Uppsala, SE |
| Decision | Substantially Equivalent, Feb 27, 2020 |
| Received | Nov 26, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193268
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.