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U.S. FDA Medical Device Microscope Stages Requirements

FDA Medical Device Definition: Microscopes and accessories are optical instruments used to enlarge images of specimens, preparations, and cultures for medical purposes. Variations of microscopes and accessories (through a change in the light source) used for medical purposes include the following:(1) Phase contrast microscopes, which permit visualization of unstained preparations by altering the phase relationship of light that passes around the object and through the object.

Registrar Corp assists Microscope Stages companies with:

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