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U.S. FDA Medical Device Disposable Medical Scissors Requirements


FDA Medical Device Definition: Medical disposable scissors are disposable type general cutting devices intended for medical purposes. This generic type of device does not include surgical scissors.

Registrar Corp assists Disposable Medical Scissors companies with:

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