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U.S. FDA Medical Device Protractor Requirements

FDA Medical Device Definition: A protractor for clinical use is a device intended for use in measuring the angles of bones, such as on x-rays or in surgery.

Registrar Corp assists Protractor companies with:

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