Registrar Corp

HomeMedical DevicesRegistration & Medical Device ListingsMedical Device Samples › U.S. FDA Lens Measuring Instrument Regulations

U.S. FDA Medical Device Lens Measuring Instrument Requirements


FDA Medical Device Definition: A lens measuring instrument is an AC-powered device intended to measure the power of lenses, prisms, and their centers (e.g., lensometer).

Registrar Corp assists Lens Measuring Instrument companies with:

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