510(k) K944837 ยท KNW Instrument, Biopsy
MEDICAL DEVICE TECHNOLOGIES MANUAL BIOPSY NEEDLE
| Applicant | Medical Device Technologies, Inc., Gainsville FL, US |
| Decision | Substantially Equivalent, Oct 14, 1994 |
| Received | Sep 30, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944837
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.