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Filing a MAF for ABS Cycolac with the U.S. FDA


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

  - VERMON USA

Registrar Corp can help you to properly prepare and submit your ABS Cycolac MAF to FDA.

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

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

For more information about filing a MAF for ABS Cycolac, 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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