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U.S. FDA Medical Device Sun Tan Booth Requirements

FDA Medical Device Definition: An ultraviolet lamp for tanning is a device that is a lamp (including a fixture) intended to provide ultraviolet radiation to tan the skin. See 1040.20 of this chapter.

Registrar Corp assists Sun Tan Booth companies with:

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