ClearanceBrief
510(k) K924200 ยท KNF Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)

REFLEX(R) ESC

ApplicantRichard-Allan Medical Ind., Inc., Richland MI, US
DecisionSubstantially Equivalent, Feb 22, 1994
ReceivedAug 20, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K924200

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.