510(k) K781641 ยท FAD Stent, Ureteral
SURGITEK DOUBLE J URETEROL STENT
| Applicant | Medical Engineering Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 7, 1978 |
| Received | Sep 21, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781641
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.