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U.S. FDA Medical Device Clitoral Engorgement Device Requirements: Clitoral Engorgement Device

FDA Medical Device Definition: A clitoral engorgement device is designed to apply a vacuum to the clitoris. It is intended for use in the treatment of female sexual arousal disorder

Registrar Corp assists Clitoral Engorgement Device companies with:

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




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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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