ClearanceBrief
510(k) K210235 ยท DQX Wire, Guide, Catheter

Verrata PLUS Pressure Guide Wire

ApplicantVolcano Corporation, San Diego CA, US
DecisionSubstantially Equivalent, Apr 15, 2021
ReceivedJan 28, 2021
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K210235

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.