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iHealth No-Touch Forehead Thermometer, Digital Infrared Thermometer for Adults and Kids, Touchless Baby Thermometer with 3 Ultra-Sensitive Sensors, Large LED Display and Gentle Vibration Alert (PT3)

$53.98

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BrandIHealth
Power SourceBattery Powered
Number of Batteries2 AAA batteries required. (included)
Response Time1 seconds

About this item

  • No Touch Measuring, Just Safe and Hygienic: PT3 Built-in infrared temperature sensor, reads body temperature within 1.18 inches of the center of the forehead without physical contact.
  • Tri-Point Sensors Accuracy: An ultra-sensitive infrared sensor collects more than 100 data points per second while distance and environmental sensors combine to account for other variables; ensuring maximum accuracy every time temperature is taken.
  • Fast, Simple, Clear and Quiet: The intuitive single-button control design thermometer reads the temperature in just 1 second from a clear bright extra-large LED screen, even in total darkness. The quiet vibration alerting ensures there is no buzzing noise and no disturbance.
  • Suitable for Multi-Scenario and All Ages: iHealth PT3 is designed for all ages: ranging from babies and toddlers to the elderly. An ideal choice for hospitals, hotels, school settings, and public establishments.
  • What You Get: 1x PT3 thermometer, 2x AAA batteries, 1x Instruction manual, 1x Quick User Guide, our worry-free 12-month warranty, and friendly California-based customer service.

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SKU: B075QQ8VZW Category:
FDA approved?Back to product
asked by admin on 2020-07-30 00:00:00
1 answers shown
  1. FDA Cleared is not the same as FDA Approved. Just because the device is "Cleared" does not mean it has been "Approved." Buyer beware - below is the terminology and it is not meant to be interchangeable:Clearance: When a medical device is cleared, this means it has undergone a 510(k) submission, which FDA has reviewed and provided clearance.Approval: For Class III medical devices to be legally marketed they must undergo a rigorous review and approval process. Following a successful submission of a premarket approval (PMA) or a Humanitarian Device Exemption (HDE), the device is given Approval by FDA. Granted: Medical devices using the De Novo pathway must be Granted by FDA before they can be legally marketed in the United States. This is a relatively new term in the FDA lexicon.
    admin answered on 2020-07-30 00:00:00

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