ClearanceBrief
510(k) K870374 ยท DYB Introducer, Catheter

PERCUTANEOUS INTRODUCER W/SIDE PORT 3 WAY STOPCOCK

ApplicantDaig Corp., Minnetonka MN, US
DecisionSubstantially Equivalent, Mar 18, 1987
ReceivedJan 29, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K870374

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.