ClearanceBrief
510(k) K802708 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

SYSTEM, ECHO, PULSED ULTRASONIC DIAG.

ApplicantGeneral Electric Co., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 7, 1981
ReceivedOct 31, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802708

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.