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U.S. FDA Medical Device Fusion & Stereoscopic Target Requirements


FDA Medical Device Definition: A fusion and stereoscopic target is a device intended for use as a viewing object with a stereoscope (886.1870).

Registrar Corp assists Fusion & Stereoscopic Target companies with:

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