ClearanceBrief
510(k) K883079 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

WWDS-005 HUMAN RECTAL PROBE

ApplicantAusonics Pty , Ltd., Suffield CT, US
DecisionSubstantially Equivalent, Dec 14, 1988
ReceivedJul 21, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883079

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.