ClearanceBrief
510(k) K820889 ยท KYG Device, Irrigation, Ocular Surgery

ASPIRATOR/IRRIGATOR OR I/A UNIT

ApplicantMid Laboratories, Inc., Walker MI, US
DecisionSubstantially Equivalent, May 5, 1982
ReceivedMar 30, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820889

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.