ClearanceBrief
510(k) K022164 ยท HKI Camera, Ophthalmic, Ac-Powered

ZETA DIAGNOSTIC RETINAL IMAGING SYSTEM

ApplicantZeta Development Laboratories, El Dorado Hills CA, US
DecisionSubstantially Equivalent, Jul 26, 2002
ReceivedJul 3, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K022164

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.