ClearanceBrief
510(k) K843972 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified

ANGIOPLUS-S

ApplicantOec-Diasonics, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Jan 3, 1985
ReceivedOct 11, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K843972

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.