ClearanceBrief
510(k) K243206 ยท IRP Massager, Powered Inflatable Tube

Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4, ACM-PLUS-A5, ACM-PLUS-A6)

ApplicantSichuan Qianli-Beoka Medical Technology, Inc., Chengdu, CN
DecisionSubstantially Equivalent, Feb 19, 2025
ReceivedOct 1, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K243206

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.