ClearanceBrief
510(k) K962584 ยท LFL Instrument, Ultrasonic Surgical

ULTRACISION 5MM HARD SHEATH LAPAROSONIC BLADE

ApplicantEthicon Endo-Surgery, Inc., Cincinnati OH, US
DecisionSubstantially Equivalent, Nov 4, 1996
ReceivedJul 1, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K962584

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.