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Filing a MAF for Acid Detergent with the U.S. FDA

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


Registrar Corp can help you to properly prepare and submit your Acid Detergent MAF to FDA.

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

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

For more information about filing a MAF for Acid Detergent, 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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