{"data":{"id":"us/21-cfr-886.1070","jurisdiction":"us","citation":"21 CFR 886.1070","heading":"Anomaloscope.","body":"(a) Identification. An anomaloscope is an AC-powered device intended to test for anomalies of color vision by displaying mixed spectral lines to be matched by the patient.\n(b) Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in § 886.9.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER H—MEDICAL DEVICES","PART 886—OPHTHALMIC DEVICES","Subpart B—Diagnostic Devices"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-21.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:24:47Z","sha256":"f25e19e18c1f1c927b7db5d03c62b0bf3db5beb484b21dd246a47adabebbb3e5","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-886.1050","next":"us/21-cfr-886.1090"},"notice":"GroundRules: Original legal text. Not legal advice."}