ClearanceBrief
510(k) K230472 ยท IMI Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat

Sonopuls 190

ApplicantEnraf-Nonius, B.V., Rotterdam, NL
DecisionSubstantially Equivalent, Oct 24, 2023
ReceivedFeb 22, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K230472

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.