ClearanceBrief
510(k) K812331 ยท HLX Photostimulator, Ac-Powered

VTS-1000 VISUAL TESTING SYSTEM

ApplicantNicolet Biomedical Instruments, Mchenry IL, US
DecisionSubstantially Equivalent, Nov 16, 1981
ReceivedAug 18, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812331

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.