510(k) K861747 ยท HPQ Headlamp, Operating, Ac-Powered
KEELER FIBEROPTIC HEADLAMP
| Applicant | Keeler Instruments, Inc., Broomall PA, US |
| Decision | Substantially Equivalent, Aug 21, 1986 |
| Received | May 6, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861747
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.