510(k) K983023 ยท DYB Introducer, Catheter
MODIFICATION TO CORDIS BRITE TIP CATHETER SHEATH INTRODUCER SYSTEM
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Oct 1, 1998 |
| Received | Aug 31, 1998 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K983023
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.