510(k) K893458 ยท EBA Light, Surgical Headlight
FIBEROPTIC HEADLIGHT SYSTEM
| Applicant | Cuda Products Co., Jacksonville FL, US |
| Decision | Substantially Equivalent, Jun 22, 1989 |
| Received | May 2, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893458
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.