510(k) K932733 ยท DYB Introducer, Catheter
CORDIS CATHETER SHEATH INTRODUCER
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Aug 26, 1993 |
| Received | Jun 7, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932733
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.