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U.S. FDA Medical Device Neurosurgical Chair Requirements

FDA Medical Device Definition: A neurosurgical chair is an operating room chair used to position and support a patient during neurosurgery.

Registrar Corp assists Neurosurgical Chair companies with:

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