ClearanceBrief
510(k) K142081 ยท DXT Injector And Syringe, Angiographic

CONTRAST MONITORING SYSTEM DISPLAY, CONTRAST MONITORING SYSTEM SYRINGES

ApplicantOsprey Medical, Inc., Minnetonka MN, US
DecisionSubstantially Equivalent, Dec 12, 2014
ReceivedJul 31, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K142081

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.