CPG Sec. 398.300 Registration of Assemblers of Diagnostic X-Ray Systems as Device Manufacturers

Name: CPG Sec. 398.300 Registration of Assemblers of Diagnostic X-Ray Systems as Device Manufacturers
Creator: Food and Drug Administration
Keywords: compliance,diagnostics,guide,manufacturers,policies,registrations,x-ray

Information

Type

Compliance Policy Guide (CPG)

Regulated products

Medical Devices, Radiation-Emitting Products

Published

February 28, 1995

Last updated

May 6, 2021

Description

This document is a Compliance Policy Guide (CPG) titled "CPG Sec. 398.300 Registration of Assemblers of Diagnostic X-Ray Systems as Device Manufacturers".

Organization

Food and Drug Administration (FDA) 🇺🇸

Country / Region

United States

License

Other (Public Domain)

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1 Main file

CPG Sec. 398.300 Registration of Assemblers of Diagnostic X-Ray Systems as Device Manufacturers

Updated on May 6, 2021

none

URL: https://www.fda.gov/regulatory-information/search-fda-guidance-documents/cpg-sec-398300-registration-assemblers-diagnostic-x-ray-systems-device-manufacturers
Permalink: https://data.openrid.co/en/datasets/r/8fbd9188-54a8-4fbc-8667-09e8e682fac6
MIME Type: None

Created on: February 28, 1995
Modified on: May 6, 2021

CPG Sec. 398.300 Registration of Assemblers of Diagnostic X-Ray Systems as Device Manufacturers

Information

Type

Regulated products

Published

Last updated

Description

Tags

Organization

Country / Region

License

Feedback

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