ClearanceBrief
510(k) K980176 ยท JAK System, X-Ray, Tomography, Computed

HISPEED QX/I CT SCANNER SYSTEM

ApplicantGeneral Electric Co., Milwaukee WI, US
DecisionSubstantially Equivalent, Apr 13, 1998
ReceivedJan 20, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K980176

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.