ClearanceBrief
510(k) K233804 ยท GEX Powered Laser Surgical Instrument

Resonic Rapid Acoustic Pulse Device

ApplicantZeltiq Aesthetics, Inc., Pleasanton CA, US
DecisionSubstantially Equivalent, Feb 1, 2024
ReceivedNov 29, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K233804

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.