510(k) K000612 ยท KNW Instrument, Biopsy
ACCUCORE SINGLE ACTION CORE BIOPSY DEVICE
| Applicant | Inrad, Kentwood MI, US |
| Decision | Substantially Equivalent, Apr 24, 2000 |
| Received | Feb 23, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000612
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.