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U.S. FDA Medical Device Powered Table Requirements

FDA Medical Device Definition: A powered table is a device intended for medical purposes that is an electrically operated flat surface table that can be 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 Powered Table companies with:

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