ClearanceBrief
510(k) K003930 ยท ELW Material, Impression

FLEXTIME MAGNUM 360

ApplicantHeraeus Kulzer, Inc., South Bend IN, US
DecisionSubstantially Equivalent, Feb 1, 2001
ReceivedDec 20, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K003930

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.