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# FDA Nixes 6 Outdated Compliance Policy Guides
- URL: https://www.fdaweb.com/fda-nixes-6-outdated-compliance-policy-guides/
- Published: 2022-04-22T12:00:00.000Z
- Updated: 2026-09-14T17:41:46.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5151662

*Federal Register* notice: FDA is withdrawing six compliance policy guides (CPGs) because they contain duplicative information or they no longer reflects the agency’s current thinking. The affected CPGs are:

· CPG Sec.500, Razor Blades, Manicuring Instruments — Not Considered Devices Under 201(h)

· CPG Sec. 310.200, Sphygmomanometers — Rx Legend

· CPG Sec. 393.100, ‘Enforcement Policy for Certain Laser Light Shows, Displays, and/or Devices

· CPG Sec. 398.425, Override of Positive Beam Limitation — 21 CFR31(g)(5)

· CPG Sec. 394.500, Importation of Television Products, Microwave Ovens, and Inherent Class 1 Laser Products for Investigation and Evaluation during Design Development

· CPG Sec. 300.750, Class 3 Devices Subject to 515(b) Requirements

To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2022-04-22/pdf/2022-08587.pdf?ref=fdaweb.com).