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U.S. FDA Medical Device Cardiovascular Intravascular Filter Requirements: Cardiovascular Intravascular Filter

FDA Medical Device Definition: A cardiovascular intravascular filter is an implant that is placed in the inferior vena cava for the purpose of preventing pulmonary thromboemboli (blood clots generated in the lower limbs and broken loose into the blood stream) from flowing into the right side of the heart and the pulmonary circulation

Registrar Corp assists Cardiovascular Intravascular Filter companies with:

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




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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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