(821 days)
e-Celsius Medical System is indicated for the measurement of core body temperature in patients for whom accurate continuous core body temperatures are clinically necessary for periods exceeding six (6) hours and with whom rectal catheters are not appropriate. e-Celsius Medical System can only be used on the order of a physician who has clinically evaluated the contraindications and warnings associated with the use of and ingestible thermometer and determined that the risk is clinically justified versus an oral thermometer or- rectal catheter.
e-Celsius Medical System is indicated for patients 18 years or older as long as their body weight is above 80 pounds.
e-Celsius Medical System is not indicated for patients with special needs, esophageal or swallowing disorders, who are psychologically unsound, or have disabilities which may make the patient unable to swallow the device for any reason, these patients should be deemed ineligible for this device.
e-Celsius Medical System is a prescription use device primarily (e.g., initial setup, final data assessment, reprocessing, etc.) indicated for use in clinical environments (e.g., hospitals, hospice, clinics, medical offices.)
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§ 880.2910 Clinical electronic thermometer.
(a)
Identification. 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.(b)
Classification. Class II (performance standards). The device is exempt from the premarket notification procedures in part 807, subpart E of this chapter, subject to the limitations in § 880.9 and the following conditions for exemption:(1) Device is not a clinical thermometer with telethermographic functions;
(2) Device is not a clinical thermometer with continuous temperature measurement functions; and
(3) Appropriate analysis and testing (such as that outlined in the currently FDA-recognized editions, as appropriate, of ISO 80601-2-56, “Medical electrical equipment—Part 2-56: Particular requirements for basic safety and essential performance of clinical thermometers for body temperature measurement,” or ASTM E1965, “Standard Specification for Infrared Thermometers for Intermittent Determination of Patient Temperature,” or ASTM E1112, “Standard Specification for Electronic Thermometer for Intermittent Determination of Patient Temperature,” or ASTM E1104, “Standard Specification for Clinical Thermometer Probe Covers and Sheaths”) must validate specifications and performance of the device.