510(k) K132995 · DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

DLP RETROGRADE CORONARY SINUS PERFUSION CANNULA WITHOUT PRESSURE MONITORING LINE, DLP RETROGRADE CORONARY SINUS PERFUSIO

Applicant	Medtronic, Inc., Minneapolis MN, US
Decision	Substantially Equivalent, Oct 31, 2013
Received	Sep 24, 2013
Type	Special
FDA record	Open on fda.gov

Recalls that name K132995

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.