ClearanceBrief
510(k) K182553 ยท DQX Wire, Guide, Catheter

Inno-Pathwire

ApplicantSuzhou Innomed Medical Device Co., Ltd., Suzhou, CN
DecisionSubstantially Equivalent, Mar 11, 2019
ReceivedSep 17, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K182553

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.