510(k) K901491 ยท FST Light, Surgical, Fiberoptic
CUDA SURGICAL LIGHT
| Applicant | Cuda Products Co., Jacksonville FL, US |
| Decision | Substantially Equivalent, Jun 18, 1990 |
| Received | Mar 29, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901491
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.