ClearanceBrief
510(k) K180709 ยท PBX Massager, Vacuum, Radio Frequency Induced Heat

truSculpt RF Device; truSculpt; truSculpt 3D

ApplicantCutera, Inc., Brisbane CA, US
DecisionSubstantially Equivalent, Jun 6, 2018
ReceivedMar 19, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K180709

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.