ClearanceBrief
510(k) K032978 ยท HNO Keratome, Ac-Powered

MODIFICATION TO CIBA VISION CENTURION SES SPIKERATOME

ApplicantCiba Vision Corporation, Duluth GA, US
DecisionSubstantially Equivalent, Oct 20, 2003
ReceivedSep 24, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K032978

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.