510(k) K101832 ยท KNW Instrument, Biopsy
BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT
| Applicant | Medical Device Technologies, Inc., Gainesville FL, US |
| Decision | Substantially Equivalent, Aug 27, 2010 |
| Received | Jul 1, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101832
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.