ClearanceBrief
510(k) K960040 ยท LFL Instrument, Ultrasonic Surgical

SHARPLAN ULTRA LAPAROSCOPIC HANDPIECE

ApplicantSharplan Lasers, Inc., Allendale NJ, US
DecisionSubstantially Equivalent, Apr 29, 1996
ReceivedJan 2, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960040

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.