ClearanceBrief
510(k) K012746 ยท LKX Device, Thermal, Hemorrhoids

ICE BATON

ApplicantBehive, Ltd., North Attleboro MA, US
DecisionSubstantially Equivalent, Nov 14, 2001
ReceivedAug 16, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K012746

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.