510(k) K934337 ยท FSW Light, Surgical, Endoscopic
CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCE
| Applicant | Cuda Products Co., Jacksonville FL, US |
| Decision | Substantially Equivalent, Nov 18, 1993 |
| Received | Sep 7, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934337
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.