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U.S. FDA Medical Device Hand-Carried Stretcher Requirements


FDA Medical Device Definition: A hand-carried stretcher is a device consisting of a lightweight frame, or of two poles with a cloth or metal platform, on which a patient can be carried.

Registrar Corp assists Hand-Carried Stretcher companies with:

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