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U.S. FDA Medical Device AC-Powered Ophthalmic Chair Requirements


FDA Medical Device Definition: An ophthalmic chair is an AC-powered or manual device with adjustable positioning in which a patient is to sit or recline during ophthalmological examination or treatment.

Registrar Corp assists AC-Powered Ophthalmic Chair companies with:

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