ClearanceBrief
510(k) K830120 ยท HRX Arthroscope

IMPROVED ARTHROSCOPE

ApplicantMarkoptic, Walker MI, US
DecisionSubstantially Equivalent, Mar 17, 1983
ReceivedJan 11, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830120

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.