510(k) K901706 ยท KZF Device, Medical Examination, Ac Powered
LIGHT, HEAD, EXAMINATION
| Applicant | Burton Medical Products Corp., Van Nuys CA, US |
| Decision | Substantially Equivalent, Jul 19, 1990 |
| Received | Apr 12, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901706
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.