Filing a MAF for Aerosol Solution with the U.S. FDA
Filing a medical device master file (MAF) for Aerosol Solution can be a useful mechanism to market your
Aerosol Solution to the U.S. Medical Device Industry. Typical Aerosol Solution producers who have filed a MAF for
Aerosol Solution include:
Registrar Corp can help you to properly prepare and submit your Aerosol Solution MAF to FDA.
As your Agent, Registrar Corp will perform the following administrative functions:
Ensure administrative accuracy of your Aerosol Solution MAF
Format, assemble and deliver your Aerosol Solution MAF to FDA
Assist with preparing letters of authorization regarding your Aerosol Solution MAF
Provide changes, additions and maintenance of your Aerosol Solution MAF
Respond to issues relating to ownership of your Aerosol Solution MAF
Assist with submission of responses to FDA concerning your Aerosol Solution MAF
For more information about filing a MAF for Aerosol Solution, 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.