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U.S. FDA Medical Device Exercise Parallel Bars Requirements


FDA Medical Device Definition: Nonmeasuring exercise equipment consist of devices intended for medical purposes, such as to redevelop muscles or restore motion to joints or for use as an adjunct treatment for obesity. Examples include a prone scooter board, parallel bars, a mechanical treadmill, an exercise table, and a manually propelled exercise bicycle.

Registrar Corp assists Exercise Parallel Bars companies with:

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