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U.S. FDA Medical Device Skiascopic Rack Requirements

FDA Medical Device Definition: A skiascopic rack is a device that is a rack and a set of attached ophthalmic lenses of various dioptric strengths intended as an aid in refraction

Registrar Corp assists Skiascopic Rack companies with:

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