510(k) K931645 ยท KZF Device, Medical Examination, Ac Powered
HALUX TASKLIGHT
| Applicant | Burton Medical Products Corp., Van Nuys CA, US |
| Decision | Substantially Equivalent, Aug 20, 1993 |
| Received | Apr 2, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931645
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.