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U.S. FDA Medical Device Slide Culture Chamber Requirements


FDA Medical Device Definition: Cell and tissue culture supplies and equipment are devices that are used to examine, propagate, nourish, or grow cells and tissue cultures. These include such articles as slide culture chambers, perfusion and roller apparatus, cell culture suspension systems, and tissue culture flasks, disks, tubes, and roller bottles

Registrar Corp assists Slide Culture Chamber companies with:

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