510(k) K050389 ยท DQY Catheter, Percutaneous
ULTRA-SOFT SV BALLOON DILATATION CATHETER
| Applicant | Boston Scientific Corp, Maple Grove MN, US |
| Decision | Substantially Equivalent, May 25, 2005 |
| Received | Feb 15, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050389
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.