Registrar Corp

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

U.S. FDA Medical Device Radiologic 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 Radiologic Table companies with:

  • FDA Radiologic Table Establishment Registration
  • FDA Radiologic Table Listing
  • FDA Radiologic Table Label Requirements and Exceptions
  • FDA Radiologic Table Import Information
  • FDA Radiologic Table Detentions (Radiologic Table Entry Refusals)
  • General U.S. Food and Drug Administration Medical Device Guidelines for:
       - Radiologic Table Manufacturers (Radiologic Table Suppliers)
       - Radiologic Table Distributors
       - Radiologic Table Processors
       - Radiologic Table Repackers
       - Radiologic Table Relabelers
       - Radiologic Table Exporters
       - Radiologic Table Importers
For more information about Radiologic 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 © 2016 Registrar Corp
Food and Beverages | Drugs | Cosmetics | Medical Devices | Radiation-Emitting Electronic Devices | Color Additives | Tobacco