ClearanceBrief
510(k) K230125 ยท GWG Endoscope, Neurological

Neuroblade System

ApplicantClearmind Biomedical, Taipei, TW
DecisionSubstantially Equivalent, Oct 13, 2023
ReceivedJan 17, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K230125

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.