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U.S. FDA Medical Device AC-Powered Surgical Chair Requirements


FDA Medical Device Definition: Operating tables and accessories and operating chairs and accessories are AC-powered or air-powered devices, usually with movable components, intended for use during diagnostic examinations or surgical procedures to support and position a patient.

Registrar Corp assists AC-Powered Surgical Chair companies with:

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