510(k) K011325 ยท FGB Ureteroscope And Accessories, Flexible/Rigid
MEDIFIX URETEROSCOPE
| Applicant | Medifix, Inc., Morton Grove IL, US |
| Decision | Substantially Equivalent, Jul 25, 2001 |
| Received | May 1, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011325
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.