510(k) K991572 ยท FST Light, Surgical, Fiberoptic
ISOLUX SURGICAL HEADLIGHT
| Applicant | Isolux America, Naples FL, US |
| Decision | Substantially Equivalent, Jul 8, 1999 |
| Received | May 5, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991572
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.