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U.S. FDA Medical Device Ophthalmic Instrument Table Requirements


FDA Medical Device Definition: An ophthalmic instrument table is an AC-powered or manual device on which ophthalmic instruments are intended to be placed.

Registrar Corp assists Ophthalmic Instrument Table companies with:

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