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U.S. FDA Medical Device Intra-Aneurysm Pressure Measurement Requirements: Intra-Aneurysm Pressure Measurement

FDA Medical Device Definition: Implantable intra-aneurysm pressure measurement system is a device used to measure the intra-sac pressure in a vascular aneurysm. The device consists of a pressure transducer that is implanted into the aneurysm and a monitor that reads the pressure from the transducer

Registrar Corp assists Intra-Aneurysm Pressure Measurement companies with:

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