ClearanceBrief
510(k) K162441 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

PowerPICC Provena Catheters with SOLO Valve Technology

ApplicantC.R. Bard, Inc., Salt Lake Ciy, UT, US
DecisionSubstantially Equivalent, Apr 24, 2017
ReceivedAug 31, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K162441

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.