ClearanceBrief
510(k) K862911 ยท ITX Transducer, Ultrasonic, Diagnostic

BI-PLANE TRANSRECTAL PROBE NUMBER H4221T

ApplicantGeneral Electric Co., Milwaukee WI, US
DecisionSubstantially Equivalent, Oct 31, 1986
ReceivedAug 1, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K862911

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.