Registrar Corp

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

U.S. FDA Medical Device Ophthalmic Aberrometer Requirements


FDA Medical Device Definition: An ophthalmic refractometer is an automatic AC-powered device that consists of a fixation system, a measurement and recording system, and an alignment system intended to measure the refractive power of the eye by measuring light reflexes from the retina.

Registrar Corp assists Ophthalmic Aberrometer companies with:

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