ClearanceBrief
510(k) K232786 ยท IPF Stimulator, Muscle, Powered

Stimulation System (PA series, PR series, S series and Q series)

ApplicantEdan Instruments, Inc., Shenzhen, CN
DecisionSubstantially Equivalent, May 16, 2024
ReceivedSep 11, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232786

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.