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U.S. FDA Medical Device Lice Combs Requirements

FDA Medical Device Definition: The lice removal kit is a comb or comb-like device intended to remove and/or kill lice and nits from head and body hair. It may or may not be battery operated.

Registrar Corp assists Lice Combs companies with:

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

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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