510(k) K910691 ยท FAD Stent, Ureteral
NORTEC URETERAL STENT
| Applicant | North American Sterilization & Packaging Co., Sparta NJ, US |
| Decision | Substantially Equivalent, Aug 15, 1991 |
| Received | Feb 19, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910691
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.