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U.S. FDA Medical Device Percussor Requirements

FDA Medical Device Definition: A percussor is a small hammerlike device used by a physician to provide light blows to a body part. A percussor is used as a diagnostic aid during physical examinations.

Registrar Corp assists Percussor companies with:

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