510(k) K011889 ยท DQY Catheter, Percutaneous
ULTRA -THIN SDS BALLOON DILATATION CATHETER
| Applicant | Boston Scientific Corp, Natick, MA, US |
| Decision | Substantially Equivalent, Dec 21, 2001 |
| Received | Jun 18, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011889
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.