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U.S. FDA Medical Device Force-Measuring Platform Requirements


FDA Medical Device Definition: A force-measuring platform is a device intended for medical purposes that converts pressure applied upon a planar surface into analog mechanical or electrical signals. This device is used to determine ground reaction force, centers of percussion, centers of torque, and their variations in both magnitude and direction with time.

Registrar Corp assists Force-Measuring Platform companies with:

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