510(k) K832378 ยท EKQ Preparer, Root Canal Endodontic
VIBRATORY ENDODONTIC SYSTEM
| Applicant | Syntex Dental Products, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 4, 1983 |
| Received | Jul 19, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832378
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.