510(k) K992483 ยท FAJ Cystoscope And Accessories, Flexible/Rigid
MEDIFIX INC.
| Applicant | Medifix, Inc., Morton Grove IL, US |
| Decision | Substantially Equivalent, Aug 30, 1999 |
| Received | Jul 26, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992483
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.