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U.S. FDA Medical Device AC-Powered Slitlamp Biomicroscope Requirements: AC-Powered Slitlamp Biomicroscope

FDA Medical Device Definition: An AC-powered slitlamp biomicroscope is an AC-powered device that is a microscope intended for use in eye examination that projects into a patient's eye through a control diaphragm a thin, intense beam of light

Registrar Corp assists AC-Powered Slitlamp Biomicroscope companies with:

  • FDA AC-Powered Slitlamp Biomicroscope Establishment Registration
  • FDA AC-Powered Slitlamp Biomicroscope Listing
  • FDA AC-Powered Slitlamp Biomicroscope Label Requirements and Exceptions
  • FDA AC-Powered Slitlamp Biomicroscope Import Information
  • FDA AC-Powered Slitlamp Biomicroscope Detentions (AC-Powered Slitlamp Biomicroscope Entry Refusals)
  • General U.S. Food and Drug Administration Medical Device Guidelines for:
       - AC-Powered Slitlamp Biomicroscope Manufacturers (AC-Powered Slitlamp Biomicroscope Suppliers)
       - AC-Powered Slitlamp Biomicroscope Distributors
       - AC-Powered Slitlamp Biomicroscope Processors
       - AC-Powered Slitlamp Biomicroscope Repackers
       - AC-Powered Slitlamp Biomicroscope Relabelers
       - AC-Powered Slitlamp Biomicroscope Exporters
       - AC-Powered Slitlamp Biomicroscope Importers
For more information about AC-Powered Slitlamp Biomicroscope Medical Devices, simply click below:




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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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