510(k) K901097 ยท DZA Drill, Dental, Intraoral
FILLOCK REAMER
| Applicant | Ivoclar North America, Inc., Amherst NY, US |
| Decision | Substantially Equivalent, Apr 25, 1990 |
| Received | Mar 7, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901097
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.