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U.S. FDA Medical Device Therapeutic Vibrator Requirements

FDA Medical Device Definition: A therapeutic vibrator is an electrically powered device intended for medical purposes that incorporates various kinds of pads and that is held in the hand or attached to the hand or to a table. It is intended for various uses, such as relaxing muscles and relieving minor aches and pains.

Registrar Corp assists Therapeutic Vibrator companies with:

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