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U.S. FDA Medical Device Electric 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 Electric Therapeutic Massager companies with:

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