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U.S. FDA Medical Device Posture Chair Requirements

FDA Medical Device Definition: A posture chair for cardiac or pulmonary treatment is a device intended to assist in the rehabilitation and mobilization of patients with chronic heart or lung disease.

Registrar Corp assists Posture Chair companies with:

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