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Filing a MAF for Antibiotic Susceptibility Discs with the U.S. FDA


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

  - LILLY RESEARCH LABORATORIES

Registrar Corp can help you to properly prepare and submit your Antibiotic Susceptibility Discs MAF to FDA.

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

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

For more information about filing a MAF for Antibiotic Susceptibility Discs, 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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