ClearanceBrief
510(k) K974112 ยท KPR System, X-Ray, Stationary

VACUDAP, MODEL 2000, 2001

ApplicantVictoreen, Inc., Solon OH, US
DecisionSubstantially Equivalent, Jan 29, 1998
ReceivedOct 31, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K974112

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.