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Filing a MAF for Acetyltri-N-Butyl Citrate with the U.S. FDA

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


Registrar Corp can help you to properly prepare and submit your Acetyltri-N-Butyl Citrate MAF to FDA.

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

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

For more information about filing a MAF for Acetyltri-N-Butyl Citrate, 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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