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U.S. FDA Medical Device C-Reactive Protein Immunological Test Requirements: C-Reactive Protein Immunological Test

FDA Medical Device Definition: A C-reactive protein immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the C-reactive protein in serum and other body fluids. Measurement of C-reactive protein aids in evaluation of the amount of injury to body tissues

Registrar Corp assists C-Reactive Protein Immunological Test companies with:

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