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U.S. FDA Medical Device Non-Electrical Surgical Chair 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 Non-Electrical Surgical Chair companies with:

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