ClearanceBrief
510(k) K972148 ยท LFL Instrument, Ultrasonic Surgical

B.U.S. ENDOTRON

ApplicantMedicamat S.A., Washington DC, US
DecisionSubstantially Equivalent, Dec 10, 1997
ReceivedJun 9, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K972148

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.