510(k) K943968 ยท MDM Instrument, Manual, Surgical, General Use
TUNNELER
| Applicant | Denver Biomedicals, Inc., Evergreen CO, US |
| Decision | Substantially Equivalent, Mar 1, 1995 |
| Received | Aug 15, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943968
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.