510(k) K932600 ยท EKX Handpiece, Direct Drive, Ac-Powered
MODIFIED SITE POWER HANDPIECE II
| Applicant | Chiron Vision Corp., Horsham PA, US |
| Decision | Substantially Equivalent, Jan 25, 1994 |
| Received | May 28, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932600
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.