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U.S. FDA Medical Device Sliding Microtome 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 Sliding Microtome companies with:

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