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U.S. FDA Medical Device TLC Developing Tanks Requirements

FDA Medical Device Definition: A thin-layer chromatography (TLC) system for clinical use is a device intended to separate one or more drugs or compounds from a mixture. The mixture of compounds is absorbed onto a stationary phase or thin layer of inert material (e.g., cellulose, alumina, etc.) and eluted off by a moving solvent (moving phase) until equilibrium occurs between the two phases.

Registrar Corp assists TLC Developing Tanks companies with:

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