Registrar Corp

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

U.S. FDA Medical Device Ophthalmic Bar Prism Requirements


FDA Medical Device Definition: An ophthalmic bar prism is a device that is a bar composed of fused prisms of gradually increasing strengths intended to measure latent and manifest strabismus (eye muscle deviation) or the power of fusion of a patient's eyes.

Registrar Corp assists Ophthalmic Bar Prism companies with:

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