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:
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.