510(k) K142125 ยท KNW Instrument, Biopsy
New Medax Biopsy Systems
| Applicant | Medax Srl Unipersonale, Poggio Rusco, IT |
| Decision | Substantially Equivalent, Dec 22, 2015 |
| Received | Aug 4, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142125
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.