Registrar Corp

HomeMedical DevicesRegistration & Medical Device ListingsMedical Device Samples › U.S. FDA Fast Green Regulations

U.S. FDA Medical Device Fast Green Requirements

FDA Medical Device Definition: Dye and chemical solution stains for medical purposes are mixtures of synthetic or natural dyes or nondye chemicals in solutions used in staining cells and tissues for diagnostic histopathology, cytopathology, or hematology.

Registrar Corp assists Fast Green companies with:

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