510(k) K974493 ยท FDS Gastroscope And Accessories, Flexible/Rigid
FIEGERT ENDOTECH FLEXIBLE FIBEROPTIC ENDOSCOPES, FIEGERT ENDOTECH FLEXIBLE VIDEO-ENDOSCOPES
| Applicant | Fiegert-Endotech Medizintechnik GmbH, Tuttlingen, DE |
| Decision | Substantially Equivalent, Mar 31, 1998 |
| Received | Nov 28, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974493
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.