510(k) K181803 ยท KNW Instrument, Biopsy
Medax Biopsy Systems III
| Applicant | Medax Srl Unipersonale, Poggio Rusco, IT |
| Decision | Substantially Equivalent, Oct 18, 2018 |
| Received | Jul 5, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181803
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.