ClearanceBrief
510(k) K855150 ยท LKX Device, Thermal, Hemorrhoids

HPK-A DEVICE DFOR THE TREATMENT OF HEMORRHOIDS

ApplicantHpk International, Inc., Washington DC, US
DecisionSubstantially Equivalent, Apr 1, 1986
ReceivedDec 26, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K855150

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.