ClearanceBrief
510(k) K861013 ยท KYG Device, Irrigation, Ocular Surgery

ELECTRICALLY CONTROLLED I.V. POLE (OPTHALMIC)

ApplicantAmeritek, Inc., Miami FL, US
DecisionSubstantially Equivalent, Mar 31, 1986
ReceivedMar 18, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K861013

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.