510(k) K111765 ยท KNW Instrument, Biopsy
FULL CORE BIOPSY SYSTEM
| Applicant | Promex Technologies, LLC, Indianapolis IN, US |
| Decision | Substantially Equivalent, Sep 6, 2011 |
| Received | Jun 23, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111765
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.