ClearanceBrief
510(k) K853135 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered

VISITEC 2 MICRON FLUID FILTER

ApplicantVisitec Co., Sarasota FL, US
DecisionSubstantially Equivalent, Aug 9, 1985
ReceivedJul 26, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K853135

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.