510(k) K910688 ยท DYB Introducer, Catheter
CORDIS PEEL-AWAY INSERTION TOOL
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, May 16, 1991 |
| Received | Feb 19, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910688
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.