ClearanceBrief
510(k) K180560 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

Sherlock 3CG+ T ip Confirmation System

ApplicantC.R. Bard, Inc., Salt Lake Ciy, UT, US
DecisionSubstantially Equivalent, Jun 18, 2018
ReceivedMar 1, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K180560

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.