ClearanceBrief
510(k) K253586 ยท HLZ Electrode, Corneal

RM Electrode (RMH 25-01)

ApplicantRetmap, Inc., Chicago IL, US
DecisionSubstantially Equivalent, Apr 1, 2026
ReceivedNov 17, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K253586

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.