ClearanceBrief
510(k) K964391 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

CHASE LEFT VENT SAFETY VALVE

ApplicantChase Medical, Inc., Richardson TX, US
DecisionSubstantially Equivalent, May 13, 1997
ReceivedNov 4, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K964391

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.