510(k) K993188 ยท EKX Handpiece, Direct Drive, Ac-Powered
ENDOSTEPPER 1
| Applicant | Phytron- Elektronik GmbH, Grobenzell, DE |
| Decision | Substantially Equivalent, Sep 28, 1999 |
| Received | Sep 23, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993188
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.