510(k) K912060 ยท FAD Stent, Ureteral
MENTOR BLACK LIGHT INJECTION STENT SET
| Applicant | Mentor Corp., Goleta CA, US |
| Decision | Substantially Equivalent, Sep 27, 1991 |
| Received | May 9, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912060
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.