510(k) K990839 ยท KNW Instrument, Biopsy
TRU-CORE I REUSABLE BIOPSY INSTRUMENT
| Applicant | Medical Device Technologies, Inc., Gainesville FL, US |
| Decision | Substantially Equivalent, May 20, 1999 |
| Received | Mar 15, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990839
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.