510(k) K942141 ยท FET Endoscopic Video Imaging System/Component, Gastroenterology-Urology
EIDOLON ENDOSCOPE COUPLER
| Applicant | Eidolon Corp., Natick MA, US |
| Decision | Substantially Equivalent, May 27, 1994 |
| Received | May 3, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942141
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.