ClearanceBrief
510(k) K120086 ยท DRA Catheter, Steerable

CARIOSOLUTIONS PERCU-PRO STEERABLE INTRODCER 65CM CARIOSOLUTIONS PERCU-PRO STEERABLE INTRODUCER 80CM

ApplicantCardiosolutions, West Bridgewater MA, US
DecisionSubstantially Equivalent, Apr 24, 2012
ReceivedJan 11, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K120086

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.