Registrar Corp

HomeMedical DevicesRegistration & Medical Device ListingsMedical Device Samples › U.S. FDA Radiographic Table Regulations

U.S. FDA Medical Device Radiographic Table Requirements

FDA Medical Device Definition: A radiologic table is a device intended for medical purposes to support a patient during radiologic procedures. The table may be fixed or tilting and may be electrically powered.

Registrar Corp assists Radiographic Table companies with:

  • FDA Radiographic Table Establishment Registration
  • FDA Radiographic Table Listing
  • FDA Radiographic Table Label Requirements and Exceptions
  • FDA Radiographic Table Import Information
  • FDA Radiographic Table Detentions (Radiographic Table Entry Refusals)
  • General U.S. Food and Drug Administration Medical Device Guidelines for:
       - Radiographic Table Manufacturers (Radiographic Table Suppliers)
       - Radiographic Table Distributors
       - Radiographic Table Processors
       - Radiographic Table Repackers
       - Radiographic Table Relabelers
       - Radiographic Table Exporters
       - Radiographic Table Importers
For more information about Radiographic Table Medical Devices, simply click below:

U.S. FDA Regulations:

U.S. FDA 510(k) Regulation: 21 C.F.R. section 814.9.

Registrar Corp assists businesses with U.S. FDA compliance. Certificates of Registration issued by Registrar Corp provide confirmation to industry that you are fulfilling U.S. FDA registration requirements. U.S. FDA does not issue or recognize Certificates of Registration. Registrar Corp is not affiliated with the U.S. Food and Drug Administration.
Home | About Us | News | Resources | Exhibitions | Seminars | Associations | Careers | Sitemap | Terms of Use © 2017 Registrar Corp
Food and Beverages | Drugs | Cosmetics | Medical Devices | Radiation-Emitting Electronic Devices | Color Additives | Tobacco