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U.S. FDA Medical Device Clinical Electronic Thermometer Requirements: Clinical Electronic Thermometer

FDA Medical Device Definition: A clinical electronic thermometer is a device used to measure the body temperature of a patient by means of a transducer coupled with an electronic signal amplification, conditioning, and display unit. The transducer may be in a detachable probe with or without a disposable cover

Registrar Corp assists Clinical Electronic Thermometer companies with:

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