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Filing a MAF for Acrylic Latex Coating with the U.S. FDA


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

  - AKRON COATINGS & ADHESIVES

Registrar Corp can help you to properly prepare and submit your Acrylic Latex Coating MAF to FDA.

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

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

For more information about filing a MAF for Acrylic Latex Coating, 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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