Nidek RS3000 Comparative Study

Inclusion Criteria: 1. Subjects of legal age and who have full legal capacity to volunteer on the date the informed consent is signed. 2. Subjects who follow the instructions by Principal/Clinical Investigator or clinical staff at the clinical site, and can visit on a scheduled examination date. 3. Subjects who sign an informed consent form to participate in the clinical study. 4. Subjects who agree to take the qualifying examination and RS-3000 and RTVue data acquisition. Exclusion Criteria: 1. Diabetes mellitus (DM) and/or diabetic retinopathy 2. Hypertension (HT) 3. Cerebral infarction, cerebral hemorrhage, cranial nerve neoplasm and other central nervous system diseases affecting vision 4. Cardiac, hepatic, renal and hematologic diseases 5. Current systemic administration of steroid 6. History of anticancer agent etc. 7. Optically-stimulated epileptic seizure 8. Dementia 9. Subjects who have other life threatening and debilitating systemic diseases NOTE: Additional detailed inclusion/exclusion ophthalmic criteria dependent upon study population also exist