ClearanceBrief
510(k) K023939 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered

VELOCITY ADVANTAGE

ApplicantVisioncare Devices, Inc., Redding CA, US
DecisionSubstantially Equivalent, Apr 17, 2003
ReceivedNov 26, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K023939

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.