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U.S. FDA Medical Device Ophthalmic Instrument Cabinet Requirements


FDA Medical Device Definition: An ophthalmic instrument stand is an AC-powered or nonpowered device intended to store ophthalmic instruments in a readily accessible position.

Registrar Corp assists Ophthalmic Instrument Cabinet companies with:

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