510(k) K992309 ยท DYB Introducer, Catheter
INTRODUCER SHEATH, VESSEL DILATOR
| Applicant | Boston Scientific Corp, San Jose CA, US |
| Decision | Unknown, Oct 7, 1999 |
| Received | Jul 9, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992309
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.