{"data":{"id":"us/42-cfr-493.1485","jurisdiction":"us","citation":"42 CFR 493.1485","heading":"Standard; Cytotechnologist responsibilities.","body":"The cytotechnologist is responsible for documenting—\n(a) The slide interpretation results of each gynecologic and nongynecologic cytology case he or she examined or reviewed (as specified in § 493.1274(c));\n(b) For each 24-hour period, the total number of slides examined or reviewed in the laboratory as well as the total number of slides examined or reviewed in any other laboratory or for any other employer; and\n(c) The number of hours spent examining slides in each 24-hour period.","path":["Title 42—Public Health","CHAPTER IV—CENTERS FOR MEDICARE \u0026 MEDICAID SERVICES, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER G—STANDARDS AND CERTIFICATION","PART 493—LABORATORY REQUIREMENTS","Subpart M—Personnel for Nonwaived Testing"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-42.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:26:11Z","sha256":"37128b3d9db524e54f1020a3de99fe0b8ae74a19a7b5f13dbc53d58898f80ac7","source_id":"us-cfr","stale":true,"prev":"us/42-cfr-493.1483","next":"us/42-cfr-493.1487"},"notice":"GroundRules: Original legal text. Not legal advice."}