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U.S. FDA Medical Device GLC Column Supports Requirements

FDA Medical Device Definition: A gas liquid chromatography system for clinical use is a device intended to separate one or more drugs or compounds from a mixture. Each of the constituents in a vaporized mixture of compounds is separated according to its vapor pressure. The device may include accessories such as columns, gases, column supports, and liquid coating.

Registrar Corp assists GLC Column Supports companies with:

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