ClearanceBrief
510(k) K050185 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

POWERHOHN AND POWERLINE CATHETERS

ApplicantC.R. Bard, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, May 26, 2005
ReceivedJan 27, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K050185

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.