ClearanceBrief
510(k) K961841 ยท FAS Electrode, Electrosurgical, Active, Urological

BARD V-MAX ROLLER BAR (3551XX;XX=01,02,03,04,05, OR 06)

ApplicantC.R. Bard, Inc., Covington GA, US
DecisionSubstantially Equivalent, Oct 9, 1996
ReceivedMay 13, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961841

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.