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U.S. FDA Medical Device Cell Culture Spinner System 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 Cell Culture Spinner System companies with:

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