510(k) K970892 ยท FAJ Cystoscope And Accessories, Flexible/Rigid
FIEGERT ENDOTECH CYSTOSCOPE
| Applicant | Fiegert, Inc., Hollywood FL, US |
| Decision | Substantially Equivalent, May 5, 1997 |
| Received | Mar 11, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970892
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.