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HHS Guidance Portal

The Guidance Portal is a public website that shows current guidance documents from the U.S. Department of Health and Human Services (HHS) and its Divisions.

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HHS Guidance Documents
Title OpDiv/StaffDiv Guidance Status Issue Date
CPG Sec. 396.300 Defective Suntanning Booths and Bed  Food and Drug Administration (FDA) Final
CPG Sec. 396.400 Policy on Warned on Sunlamp Products  Food and Drug Administration (FDA) Final
CPG Sec. 398.100 Definition of General Purpose Radiographic X-Ray System - 21 CFR 1020.30(b)  Food and Drug Administration (FDA) Final
CPG Sec. 398.200 Hazardous Diagnostic X-ray Systems  Food and Drug Administration (FDA) Final
CPG Sec. 398.300 Registration of Assemblers of Diagnostic X-Ray Systems as Device Manufacturers  Food and Drug Administration (FDA) Final
CPG Sec. 398.325 Regulatory Actions Against Assemblers Noncompliant Diagnostic X-Ray Equipment  Food and Drug Administration (FDA) Final
CPG Sec. 398.375 Obligations of Factory-based Manufacturers and Assemblers of Diagnostic X-ray Equipment Under the Performance Standard for Diagnostic X-ray Equipment  Food and Drug Administration (FDA) Final
CPG Sec. 398.400 Automatic Adjustment of the X-ray Field Size to the Selected Spot-Film Size - 21 CFR 1020.31(g)(1)  Food and Drug Administration (FDA) Final
CPG Sec. 398.450 Applicability of Positive Beam Limitation (PBL) Requirements When PBL is Provided on "Other than Stationary General Purpose" Radiographic System  Food and Drug Administration (FDA) Final
CPG Sec. 398.600 Certification and Identification of X-ray Components - Sections 1010.2 and 1020.30(e)  Food and Drug Administration (FDA) Final
This Guidance Portal contains 4735 documents.