ClearanceBrief
510(k) K192921 ยท HRX Arthroscope

Zeos Aqua Vision Pump and tube

ApplicantHemodia Sas, Labege, FR
DecisionSubstantially Equivalent, Oct 9, 2020
ReceivedOct 16, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K192921

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.