510(k) K894430 ยท DYB Introducer, Catheter
MODIFIED LABEL TO PERCU. INTRO. W/SIDEPORT & 3-WAY
| Applicant | Daig Corp., Minnetonka MN, US |
| Decision | Substantially Equivalent, Aug 9, 1989 |
| Received | Jul 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894430
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.