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U.S. FDA Medical Device Ocular Esthesiometer Requirements


FDA Medical Device Definition: An ocular esthesiometer is a device, such as a single-hair brush, intended to touch the cornea to assess corneal sensitivity.

Registrar Corp assists Ocular Esthesiometer companies with:

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