510(k) K900082 ยท KNW Instrument, Biopsy
MAXX 470 CORE BIOPSY GUN
| Applicant | Dlp, Inc., Grand Rapids MI, US |
| Decision | Substantially Equivalent, Jun 27, 1990 |
| Received | Jan 5, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900082
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.