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

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> FDA guidance document: CPG Sec. 398.700 Reloaders of X-ray Tube Housing Assemblies; Applicability of Medical Device Establishment Registration, Device Listing and Biennial Inspection. Issue date: February 28, 2005. Get complete insights and analysis.

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## Details

- Title: CPG Sec. 398.700 Reloaders of X-ray Tube Housing Assemblies; Applicability of Medical Device Establishment Registration, Device Listing and Biennial Inspection
- Communication Type: Guidance Document
- Product Type: Radiation-Emitting Products, Medical Devices
- Office Name: Office of Regulatory Affairs
- Issue Date: 2005-02-28

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