ClearanceBrief
510(k) K063531 ยท LFL Instrument, Ultrasonic Surgical

SERIES 3 LOTUS LAPAROSCOPIC ULTRASOUND SURGERY SYSTEM

ApplicantSra Developments, Ltd., Ashburton, Devon, GB
DecisionSubstantially Equivalent, Feb 22, 2007
ReceivedNov 22, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K063531

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.