510(k) K990278 ยท KNW Instrument, Biopsy
DAUM NEUROCUT NEUROBIOPSYNEEDLE
| Applicant | Daum Corp., Crofton MD, US |
| Decision | Substantially Equivalent, Mar 30, 1999 |
| Received | Jan 28, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990278
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.