ClearanceBrief
510(k) K221102 ยท LFL Instrument, Ultrasonic Surgical

LOTUS Series 4 Enhanced Shears, LOTUS Series 5

ApplicantSra Developments, Ltd., Ashburton, GB
DecisionSubstantially Equivalent, Dec 15, 2022
ReceivedApr 14, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K221102

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.