510(k) K893491 ยท FST Light, Surgical, Fiberoptic
MODEL M2-150/I-150/M2-150T/M3-150/M2-150,300-300
| Applicant | Cuda Products Co., Jacksonville FL, US |
| Decision | Substantially Equivalent, Jun 22, 1989 |
| Received | May 4, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893491
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.