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U.S. FDA Medical Device Nearpoint (Punctometer) Ruler Requirements

FDA Medical Device Definition: A nearpoint ruler is a device calibrated in centimeters intended to measure the nearpoint of convergence (the point to which the visual lines are directed when convergence is at its maximum).

Registrar Corp assists Nearpoint (Punctometer) Ruler companies with:

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