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U.S. FDA Medical Device Nasopharyngeal Airway Requirements


FDA Medical Device Definition: A nasopharyngeal airway is a device used to aid breathing by means of a tube inserted into a patient's pharynx through the nose to provide a patent airway.

Registrar Corp assists Nasopharyngeal Airway companies with:

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