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U.S. FDA Medical Device Deodorized Menstrual Tampon Requirements: Deodorized Menstrual Tampon

FDA Medical Device Definition: A scented or scented deodorized menstrual tampon is a device that is a plug made of cellulosic or synthetic material that is inserted into the vagina and used to absorb menstrual or other vaginal discharge. It has scent (i.e., fragrance materials) added for aesthetic purposes (scented menstrual tampon) or for deodorizing purposes (scented deodorized menstrual tampon). This generic type of device does not include menstrual tampons treated with added antimicrobial agents or other drugs

Registrar Corp assists Deodorized Menstrual Tampon companies with:

  • FDA Deodorized Menstrual Tampon Establishment Registration
  • FDA Deodorized Menstrual Tampon Listing
  • FDA Deodorized Menstrual Tampon Label Requirements and Exceptions
  • FDA Deodorized Menstrual Tampon Import Information
  • FDA Deodorized Menstrual Tampon Detentions (Deodorized Menstrual Tampon Entry Refusals)
  • General U.S. Food and Drug Administration Medical Device Guidelines for:
       - Deodorized Menstrual Tampon Manufacturers (Deodorized Menstrual Tampon Suppliers)
       - Deodorized Menstrual Tampon Distributors
       - Deodorized Menstrual Tampon Processors
       - Deodorized Menstrual Tampon Repackers
       - Deodorized Menstrual Tampon Relabelers
       - Deodorized Menstrual Tampon Exporters
       - Deodorized Menstrual Tampon Importers
For more information about Deodorized Menstrual Tampon Medical Devices, 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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