ClearanceBrief
510(k) K853961 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered

VISITEC OPHTHALMIC ASPIRATION UNIT MODEL 100

ApplicantVisitec Co., Sarasota FL, US
DecisionSubstantially Equivalent, Dec 13, 1985
ReceivedSep 25, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K853961

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.