510(k) K882157 ยท FAD Stent, Ureteral
PANAMEX(TM) URETERAL STENT
| Applicant | Kingston Technologies, Inc., Dayton NJ, US |
| Decision | Substantially Equivalent, Aug 2, 1988 |
| Received | May 23, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882157
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.