ClearanceBrief
510(k) K880714 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

DIASONICS QT ENDORECTAL 7.5 MHZ PROBE

ApplicantDiasonics, Inc., Milipitas CA, US
DecisionSubstantially Equivalent, Apr 21, 1988
ReceivedFeb 22, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880714

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.