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U.S. FDA Medical Device Cannabinoid Test System Requirements: Cannabinoid Test System

FDA Medical Device Definition: A cannabinoid test system is a device intended to measure any of the cannabinoids, hallucinogenic compounds endogenous to marihuana, in serum, plasma, saliva, and urine. Cannabinoid compounds includedelta -9-tetrahydrocannabinol, cannabidiol, cannabinol, and cannabichromene. Measurements obtained by this device are used in the diagnosis and treatment of cannabinoid use or abuse and in monitoring levels of cannabinoids during clinical investigational use

Registrar Corp assists Cannabinoid Test System companies with:

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