510(k) K000416 ยท MPA Endoilluminator
TRANSPAK (VITREORETINAL INFUSION PAK), MODELS 90000, 90001
| Applicant | Retinalabs.Com, Atlanta GA, US |
| Decision | Substantially Equivalent, May 8, 2000 |
| Received | Feb 8, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000416
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.