510(k) K202012 ยท KNW Instrument, Biopsy
Mammotome Revolve Dual Vacuum Assisted Biopsy (VAB) System
| Applicant | Devicor Medical Products, Inc., Cincinnati OH, US |
| Decision | Substantially Equivalent, Aug 18, 2020 |
| Received | Jul 21, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202012
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.