510(k) K960323 ยท FGB Ureteroscope And Accessories, Flexible/Rigid
KARL STORZ GELET URETERO-RENOSCOPES/KARL STORZ ALKEN MOTION CONTROL DEVICE
| Applicant | KARL STORZ Endoscopy-America, Inc., Culver City CA, US |
| Decision | Substantially Equivalent, Apr 22, 1996 |
| Received | Jan 23, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960323
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.