Registrar Corp

HomeMedical DevicesRegistration & Medical Device ListingsMedical Device Samples › U.S. FDA AC-Powered Maxwell Spot Regulations

U.S. FDA Medical Device AC-Powered Maxwell Spot Requirements


FDA Medical Device Definition: A Maxwell spot is an AC-powered device that is a light source with a red and blue filter intended to test macular function.

Registrar Corp assists AC-Powered Maxwell Spot companies with:

  • FDA AC-Powered Maxwell Spot Establishment Registration
  • FDA AC-Powered Maxwell Spot Listing
  • FDA AC-Powered Maxwell Spot Label Requirements and Exceptions
  • FDA AC-Powered Maxwell Spot Import Information
  • FDA AC-Powered Maxwell Spot Detentions (AC-Powered Maxwell Spot Entry Refusals)
  • General U.S. Food and Drug Administration Medical Device Guidelines for:
       - AC-Powered Maxwell Spot Manufacturers (AC-Powered Maxwell Spot Suppliers)
       - AC-Powered Maxwell Spot Distributors
       - AC-Powered Maxwell Spot Processors
       - AC-Powered Maxwell Spot Repackers
       - AC-Powered Maxwell Spot Relabelers
       - AC-Powered Maxwell Spot Exporters
       - AC-Powered Maxwell Spot Importers
For more information about AC-Powered Maxwell Spot 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.
Home | About Us | News | Resources | Exhibitions | Seminars | Associations | Careers | Sitemap | Terms of Use © 2016 Registrar Corp
 
Food and Beverages | Drugs | Cosmetics | Medical Devices | Radiation-Emitting Electronic Devices | Color Additives | Tobacco