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U.S. FDA Medical Device Interconnected Metal Sound Requirements


FDA Medical Device Definition: An interlocking urethral sound is a device that consists of two metal sounds (elongated instruments for exploring or sounding body cavities) with interlocking ends, such as with male and female threads or a rounded point and mating socket, used in the repair of a ruptured urethra. The device may include a protective cap to fit over the metal threads.

Registrar Corp assists Interconnected Metal Sound companies with:

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