ClearanceBrief
510(k) K953526 ยท LFC Device, Caries Detection

SEEK

ApplicantUltradent Products, Inc., South Jordan UT, US
DecisionSubstantially Equivalent, Sep 5, 1995
ReceivedJul 27, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K953526

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.