U.S. FDA Medical Device TLC Light U.V. 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.
FDA TLC Light U.V. Label Requirements and Exceptions
FDA TLC Light U.V. Import Information
FDA TLC Light U.V. Detentions (TLC Light U.V. Entry Refusals)
General U.S. Food and Drug Administration Medical Device Guidelines for:
- TLC Light U.V. Manufacturers (TLC Light U.V. Suppliers)
- TLC Light U.V. Distributors
- TLC Light U.V. Processors
- TLC Light U.V. Repackers
- TLC Light U.V. Relabelers
- TLC Light U.V. Exporters
- TLC Light U.V. Importers
For more information about TLC Light U.V. Medical Devices, simply click below:
U.S. FDA Regulations:
U.S. FDA 510(k) Regulation: 21 C.F.R. section 814.9.
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