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Filing a MAF for Argon Laser with the U.S. FDA

Filing a medical device master file (MAF) for Argon Laser can be a useful mechanism to market your Argon Laser to the U.S. Medical Device Industry. Typical Argon Laser producers who have filed a MAF for Argon Laser include:


Registrar Corp can help you to properly prepare and submit your Argon Laser MAF to FDA.

As your Agent, Registrar Corp will perform the following administrative functions:

  - Ensure administrative accuracy of your Argon Laser MAF
  - Format, assemble and deliver your Argon Laser MAF to FDA
  - Assist with preparing letters of authorization regarding your Argon Laser MAF
 - Provide changes, additions and maintenance of your Argon Laser MAF
  - Respond to issues relating to ownership of your Argon Laser MAF
  - Assist with submission of responses to FDA concerning your Argon Laser MAF

For more information about filing a MAF for Argon Laser, simply click below:

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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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