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U.S. FDA Medical Device Corticoids Radioimmunoassay Requirements


FDA Medical Device Definition: A corticoids test system is a device intended to measure the levels of corticoids (hormones of the adrenal cortex) in serum and p lasma. Measurements of corticoids are used in the diagnosis and treatment of disorders of the cortex of the adrenal glands, especially those associated with hypertension and electrolyte disturbances.

Registrar Corp assists Corticoids Radioimmunoassay companies with:

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