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Federal regulations · Through 2026-08-25 · Newer source version available

21 CFR 801.6: Medical devices; misleading statements.

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Where this section sits in the code
  1. Title 21—Food and Drugs
  2. CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  3. SUBCHAPTER H—MEDICAL DEVICES
  4. PART 801—LABELING
  5. Subpart A—General Labeling Provisions

Among representations in the labeling of a device which render such device misbranded is a false or misleading representation with respect to another device or a drug or food or cosmetic.

Collected 2026-08-27T02:24:47Z. Source file · JSON

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