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U.S. FDA Medical Device Surgical Table Cushion Requirements


FDA Medical Device Definition: A manual operating table and accessories and a manual operating chair and accessories are nonpowered devices, usually with movable components, intended to be used to support a patient during diagnostic examinations or surgical procedures.

Registrar Corp assists Surgical Table Cushion companies with:

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