ClearanceBrief
510(k) K160190 ยท DXT Injector And Syringe, Angiographic

Sunmed Control Syringes

ApplicantSunny Medical Device (Shenzhen) Co., Ltd., Irvine CA, US
DecisionSubstantially Equivalent, Nov 10, 2016
ReceivedJan 27, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K160190

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.