ClearanceBrief
510(k) K864222 ยท ITX Transducer, Ultrasonic, Diagnostic

SERIES 620 RECTAL PROBE COVER

ApplicantGeneral Electric Co., Milwaukee WI, US
DecisionSubstantially Equivalent, Mar 4, 1987
ReceivedOct 28, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K864222

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.