Registrar Corp

HomeMedical Devices510(k) Administrative ReviewMedical Device 510(k) Examples › U.S. FDA Central Nervous System Fluid Shunt and Components Regulations

U.S. FDA Medical Device Central Nervous System Fluid Shunt and Components Requirements: Central Nervous System Fluid Shunt and Components

FDA Medical Device Definition: A central nervous system fluid shunt is a device or combination of devices used to divert fluid from the brain or other part of the central nervous system to an internal delivery site or an external receptacle for the purpose of relieving elevated intracranial pressure or fluid volume (e.g., due to hydrocephalus). Components of a central nervous system shunt include catheters, valved catheters, valves, connectors, and other accessory components intended to facilitate use of the shunt or evaluation of a patient with a shunt

Registrar Corp assists Central Nervous System Fluid Shunt and Components companies with:

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




Live Help

 
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.
Home | About Us | News | Resources | Exhibitions | Seminars | Associations | Careers | Sitemap | Terms of Use © 2016 Registrar Corp
 
Food and Beverages | Drugs | Cosmetics | Medical Devices | Radiation-Emitting Electronic Devices | Color Additives | Tobacco