510(k) K931102 ยท DYB Introducer, Catheter
CORDIS NIHON CATHETER SHEATH INTRODUCER
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, May 27, 1993 |
| Received | Mar 3, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931102
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.