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U.S. FDA Medical Device Oxygen Nasal Cannula Requirements


FDA Medical Device Definition: A nasal oxygen cannula is a two-pronged device used to administer oxygen to a patient through both nostrils.

Registrar Corp assists Oxygen Nasal Cannula companies with:

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