ClearanceBrief
510(k) K131770 ยท DQO Catheter, Intravascular, Diagnostic

PRESSURE CONNECTING TUBE

ApplicantShenzhen Ant Hi-Tech Industrial Co., Ltd., Dongguan, CN
DecisionSubstantially Equivalent, Feb 26, 2014
ReceivedJun 17, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K131770

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.