510(k) K020848 ยท KNW Instrument, Biopsy
NAFD 100
| Applicant | Neomatrix, LLC, Irvine CA, US |
| Decision | Substantially Equivalent, Sep 23, 2002 |
| Received | Mar 15, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020848
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.