ClearanceBrief
510(k) K212035 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

FibroScan 230

ApplicantEchosens, Paris, FR
DecisionSubstantially Equivalent, Jul 30, 2021
ReceivedJun 30, 2021
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K212035

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.