510(k) K910861 ยท DYB Introducer, Catheter
PERCUTANEOUS INTROD W/SIDEPORT/THREE-WAY STOPCOCK
| Applicant | Daig Corp., Minnetonka MN, US |
| Decision | Substantially Equivalent, May 7, 1991 |
| Received | Feb 15, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910861
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.