510(k) K991366 ยท KNW Instrument, Biopsy
DAUM MRI/CONVENTIONAL BIOPSY KIT
| Applicant | Daum GmbH, Crofton MD, US |
| Decision | Substantially Equivalent, Jun 25, 1999 |
| Received | Apr 20, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991366
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.