510(k) K092338 ยท KNW Instrument, Biopsy
MEDAX UNIPERSONALE SRL
| Applicant | Medax Unipersonale Srl, Doral FL, US |
| Decision | Substantially Equivalent, May 27, 2011 |
| Received | Aug 4, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092338
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.