510(k) K013921 ยท FAD Stent, Ureteral
PORGES SILICONE DOUBLE LOOP URETERAL STENT, MODEL # AJ4X / BJ1X / BJ2X
| Applicant | Porges S.A., Le Plessis Robinson Cedex, FR |
| Decision | Substantially Equivalent, Oct 17, 2002 |
| Received | Nov 27, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013921
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.