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U.S. FDA Medical Device Vein Stabilization Device Requirements


FDA Medical Device Definition: A vein stabilizer is a device consisting of a flat piece of plastic with two noninvasive prongs. The device is placed on the skin so that the prongs are on either side of a vein and hold it stable while a hypodermic needle is inserted into the vein

Registrar Corp assists Vein Stabilization Device companies with:

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