ClearanceBrief
510(k) K240788 ยท IMI Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat

Ultrasound Stimulator

ApplicantJkh Health Co., Ltd., Shenzhen, CN
DecisionSubstantially Equivalent, Jun 4, 2025
ReceivedMar 22, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K240788

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.