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U.S. FDA Medical Device Fluorescence Wood'S Light Requirements


FDA Medical Device Definition: A Wood's fluorescent lamp is a device intended for medical purposes to detect fluorescent materials (e.g., fluorescein pigment produced by certain microorganisms) as an aid in the identification of these microorganisms. The device aids in the diagnosis of disease.

Registrar Corp assists Fluorescence Wood'S Light companies with:

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