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U.S. FDA Medical Device Microscope Slides Requirements


FDA Medical Device Definition: Tissue processing equipment consists of devices used to prepare human tissue specimens for diagnostic histological examination by processing specimens through the various stages of decalcifying, infiltrating, sectioning, and mounting on microscope slides.

Registrar Corp assists Microscope Slides companies with:

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