510(k) K072989 ยท EFB Handpiece, Air-Powered, Dental
AXIS SYSTEM
| Applicant | Dentsply Intl., Inc., York PA, US |
| Decision | Substantially Equivalent, Jan 28, 2008 |
| Received | Oct 23, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072989
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.