510(k) K974448 ยท DYB Introducer, Catheter
CORDIS BRITE TIP CATHETER SHEATH INTRODUCER SYSTEM
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Feb 6, 1998 |
| Received | Nov 25, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974448
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.