FDA Nixes 6 Outdated Compliance Policy Guides

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.