510(k) K954265 ยท KNW Instrument, Biopsy
TROCAR STYLE NEEDLE/CO-AXIAL INTRODUCER NEEDLE
| Applicant | Promex, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Sep 29, 1995 |
| Received | Sep 12, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954265
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.