Home/CFR/Title 21/Part 812/§ 812.80
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§ 812.80 — Not Yet Available

21 C.F.R. § 812.80

21 C.F.R. § 812.80 is referenced in other legal documents but could not be loaded from the eCFR.

This section may have been removed, reserved, or renumbered. Browse Part 812 or Title 21 — Food and Drugs for available sections.

Nearby Sections

15
§ 812.1
Scope.
§ 812.2
Applicability.
§ 812.3
Definitions.
§ 812.5
Labeling of investigational devices.
§ 812.7
Prohibition of promotion and other practices.
§ 812.10
Waivers.
§ 812.18
Import and export requirements.
§ 812.19
Address for IDE correspondence.
§ 812.20
Application.
§ 812.25
Investigational plan.
§ 812.27
Report of prior investigations.
§ 812.28
Acceptance of data from clinical investigations conducted outside the United States.
§ 812.30
FDA action on applications.
§ 812.35
Supplemental applications.
§ 812.36
Treatment use of an investigational device.