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U.S. FDA Medical Device Slide Warming Table 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 Slide Warming Table companies with:

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