Registrar Corp

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

U.S. FDA Medical Device Mechanical Table Requirements

FDA Medical Device Definition: A mechanical table is a device intended for medical purposes that has a flat surface that can be inclined or adjusted to various positions. It is used by patients with circulatory, neurological, or musculoskeletal conditions to increase tolerance to an upright or standing position.

Registrar Corp assists Mechanical Table companies with:

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