ClearanceBrief
510(k) K022354 ยท JAK System, X-Ray, Tomography, Computed

ULTRAGUIDE CTG 2000SA

ApplicantUltraguide , Ltd., Hasbrouck Heights NJ, US
DecisionSubstantially Equivalent, Aug 13, 2002
ReceivedJul 19, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K022354

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.