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U.S. FDA Medical Device AC-Powered Automatic Perimeter Requirements


FDA Medical Device Definition: A perimeter is an AC-powered or manual device intended to determine the extent of the peripheral visual field of a patient. The device projects light on various points of a curved surface, and the patient indicates whether he or she sees the light.

Registrar Corp assists AC-Powered Automatic Perimeter companies with:

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