510(k) K893992 ยท KNW Instrument, Biopsy
NOETIX, BIOPSY NEEDLE
| Applicant | Noetix, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Sep 8, 1989 |
| Received | Jun 5, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893992
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.