CPG Sec. 398.700 Reloaders of X-ray Tube Housing Assemblies; Applicability of Medical Device Establishment Registration, Device Listing and Biennial Inspection

Name: CPG Sec. 398.700 Reloaders of X-ray Tube Housing Assemblies; Applicability of Medical Device Establishment Registration, Device Listing and Biennial Inspection
Creator: Food and Drug Administration
Keywords: device-listing,establishment,guidances,inspection,medical-devices,registrations,requirements,x-ray

Information

Type

Guidance

Regulated products

Medical Devices, Radiation-Emitting Products

Published

February 28, 2005

Last updated

December 1, 2018

Description

CPG Sec. 398.700 provides guidance on the registration and inspection requirements for reloaders of X-ray tube housing assemblies.

Organization

Food and Drug Administration (FDA) 🇺🇸

Country / Region

United States

License

Other (Public Domain)

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CPG Sec. 398.700 Reloaders of X-ray Tube Housing Assemblies; Applicability of Medical Device Establishment Registration, Device Listing and Biennial Inspection

Updated on December 1, 2018

none

URL: https://www.fda.gov/regulatory-information/search-fda-guidance-documents/cpg-sec-398700-reloaders-x-ray-tube-housing-assemblies-applicability-medical-device-establishment
Permalink: https://data.openrid.co/en/datasets/r/0920bf4c-b3b3-4c7e-8ca0-09b1bbda97b8
MIME Type: None

Created on: February 28, 2005
Modified on: December 1, 2018

CPG Sec. 398.700 Reloaders of X-ray Tube Housing Assemblies; Applicability of Medical Device Establishment Registration, Device Listing and Biennial Inspection

Information

Type

Regulated products

Published

Last updated

Description

Tags

Organization

Country / Region

License

Feedback

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