510(k) K922349 ยท KOE Dilator, Urethral
DOWD(TM) II
| Applicant | Boston Scientific Corp, Watertown MA, US |
| Decision | Substantially Equivalent, Aug 14, 1992 |
| Received | May 19, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922349
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.