510(k) K931785 ยท DZE Implant, Endosseous, Root-Form
BRANEMARK SYSTEM DRILL CONTROLLER
| Applicant | Nobelpharma USA, Inc., Chicago IL, US |
| Decision | Substantially Equivalent, Aug 9, 1994 |
| Received | Apr 9, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931785
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.