510(k) K964555 ยท MPA Endoilluminator
VITROTEC TRUE LIGHT ENDOILLUMINATOR (100-S)
| Applicant | Vitrotec, Inc., Chesterfield MO, US |
| Decision | Substantially Equivalent, Mar 31, 1997 |
| Received | Nov 13, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964555
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.