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U.S. FDA Medical Device Manual Therapeutic Massager Requirements


FDA Medical Device Definition: A therapeutic massager is an electrically powered device intended for medical purposes, such as to relieve minor muscle aches and pains.

Registrar Corp assists Manual Therapeutic Massager companies with:

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