Registrar Corp

HomeMedical DevicesRegistration & Medical Device ListingsMedical Device Samples › U.S. FDA Ophthalmic Projector Regulations

U.S. FDA Medical Device Ophthalmic Projector Requirements


FDA Medical Device Definition: An ophthalmic projector is an AC-powered device intended to project an image on a screen for vision testing.

Registrar Corp assists Ophthalmic Projector companies with:

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