ClearanceBrief
510(k) K820026 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered

VITRE CON

ApplicantMedical Instrument Development Laboratories, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 5, 1982
ReceivedJan 5, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820026

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.