ClearanceBrief
510(k) K832703 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered

ARGON LASER SYS-MODEL 5000

ApplicantCooper Medical Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 30, 1984
ReceivedAug 11, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832703

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.