ClearanceBrief
510(k) K837046 ยท

AUTOFOCUS PROBE FOR USE WITH ULTRASOUND AUTOSECTOR SYSTEM

ApplicantTechnicare Corp., Solon OH, US
DecisionSubstantially Equivalent, Apr 1, 1983
ReceivedJan 10, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K837046

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.