510(k) K962969 ยท KNW Instrument, Biopsy
MEDICAL DEVICE TECHNOLOGIES, INC.ULTRA
| Applicant | Medical Device Technologies, Inc., Gainsville FL, US |
| Decision | Substantially Equivalent, Dec 6, 1996 |
| Received | Jul 31, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962969
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.