§801.1. Medical devices; name and place of business of manufacturer, packer or distributor. — Inbound Citations
21 C.F.R. § 801.1
Statutory Authority
Cited by 2 regulations in release Current.
Citations to 21 C.F.R. § 801.1 as a whole
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(a) An investigational device or its immediate package shall bear a label with the following information: the name and place of business of the manufacturer, packer, or distributor (in accordance with § 801.1), the quantity of contents, if appropriate, and the following statement: “CAUTION—Investigational device. Limited by Federal (or United States) law to investigational use.” The label or other labeling shall describe all relevant contraindications, hazards, adverse effects, interfering substances or devices, warnings, and precautions.
Citations to §801.1(d)
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(1) § 801.1(d);