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42 CFR 493.1485

§ 493.1485 Standard; Cytotechnologist responsibilities.

United States · 42 CFR — Public Health · Status: effective

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42 CFR 493.1485, § 493.1485 Standard; Cytotechnologist responsibilities, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/207908
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The cytotechnologist is responsible for documenting— (a) The slide interpretation results of each gynecologic and nongynecologic cytology case he or she examined or reviewed (as specified in § 493.1274(c)); (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 (c) The number of hours spent examining slides in each 24-hour period.

Legislative history

This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.