ClearanceBrief
510(k) K883238 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

GENESIS II TRANSCRANIAL PROBE

ApplicantBiosound, Inc., Indianapolis IN, US
DecisionSubstantially Equivalent, Aug 24, 1988
ReceivedAug 1, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883238

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.