510(k) K932719 ยท KZF Device, Medical Examination, Ac Powered
RITTER MODEL 158 AND 159 EXAM LIGHTS
| Applicant | Midmark Corp., Versailles OH, US |
| Decision | Substantially Equivalent, Dec 2, 1993 |
| Received | Jun 4, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932719
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.