Registrar Corp

HomeMedical DevicesRegistration & Medical Device ListingsMedical Device Samples › U.S. FDA Nose Clip Regulations

U.S. FDA Medical Device Nose Clip Requirements

FDA Medical Device Definition: A nose clip is a device intended to close a patient's external nares (nostrils) during diagnostic or therapeutic procedures.

Registrar Corp assists Nose Clip companies with:

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