510(k) K925080 ยท EFB Handpiece, Air-Powered, Dental
TEK-LUBE
| Applicant | Clinical Technology Corp., Scottsdale AZ, US |
| Decision | Substantially Equivalent, Jan 31, 1994 |
| Received | Oct 7, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925080
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.