ClearanceBrief
510(k) K884556 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered

DREYER CURVED ENDOILLUMINATOR

ApplicantAdvanced Surgical Products, Inc., Chesterfield MO, US
DecisionSubstantially Equivalent, Feb 28, 1989
ReceivedOct 31, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884556

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.