510(k) K960148 ยท FAD Stent, Ureteral
CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENT
| Applicant | Cabot Medical Corp., Langhorne PA, US |
| Decision | Substantially Equivalent, Mar 25, 1996 |
| Received | Jan 11, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960148
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.