Registrar Corp

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

U.S. FDA Medical Device Aneurysm Clip Requirements: Aneurysm Clip

FDA Medical Device Definition: An aneurysm clip is a device used to occlude an intracranial aneurysm (a balloonlike sac formed on a blood vessel) to prevent it from bleeding or bursting

Registrar Corp assists Aneurysm Clip companies with:

  • FDA Aneurysm Clip Establishment Registration
  • FDA Aneurysm Clip Listing
  • FDA Aneurysm Clip Label Requirements and Exceptions
  • FDA Aneurysm Clip Import Information
  • FDA Aneurysm Clip Detentions (Aneurysm Clip Entry Refusals)
  • General U.S. Food and Drug Administration Medical Device Guidelines for:
       - Aneurysm Clip Manufacturers (Aneurysm Clip Suppliers)
       - Aneurysm Clip Distributors
       - Aneurysm Clip Processors
       - Aneurysm Clip Repackers
       - Aneurysm Clip Relabelers
       - Aneurysm Clip Exporters
       - Aneurysm Clip Importers
For more information about Aneurysm Clip 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 © 2016 Registrar Corp
 
Food and Beverages | Drugs | Cosmetics | Medical Devices | Radiation-Emitting Electronic Devices | Color Additives | Tobacco