Registrar Corp

HomeMedical Devices510(k) Administrative ReviewMedical Device 510(k) Examples › U.S. FDA Arthroscope Regulations

U.S. FDA Medical Device Arthroscope Requirements: Arthroscope

FDA Medical Device Definition: An arthroscope is an electrically powered endoscope intended to make visible the interior of a joint. The arthroscope and accessories also is intended to perform surgery within a joint

Registrar Corp assists Arthroscope companies with:

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

Live Help

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.
Home | About Us | News | Resources | Exhibitions | Seminars | Associations | Careers | Sitemap | Terms of Use © 2017 Registrar Corp
Food and Beverages | Drugs | Cosmetics | Medical Devices | Radiation-Emitting Electronic Devices | Color Additives | Tobacco