ClearanceBrief
510(k) K020911 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered

MID LABS AUTONOMOUS VIT ENHANCER (AVE)

ApplicantMedical Instrument Development Laboratories, Inc., San Leandro CA, US
DecisionSubstantially Equivalent, Apr 29, 2002
ReceivedMar 20, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K020911

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.