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Title 42 Part 493 → Subpart M → §493.1485

Title 42 → Chapter IV → Subchapter G → Part 493 → Subpart M → §493.1485

Electronic Code of Federal Regulations e-CFR

Title 42 Part 493 → Subpart M → §493.1485

e-CFR data is current as of January 16, 2020

Title 42Chapter IVSubchapter GPart 493Subpart M → §493.1485


Title 42: Public Health
PART 493—LABORATORY REQUIREMENTS
Subpart M—Personnel for Nonwaived Testing


§493.1485   Standard; Cytotechnologist responsibilities.

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.

[57 FR 7172, Feb. 28, 1992, as amended at 68 FR 3714, Jan. 24, 2003]