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FDA 510(k)

Microlife Digital Infrared Ear Thermometer

K-Number: K170219 · 2017-07-20

Decision Date2017-07-20
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Microlife Digital Infrared Ear Thermometer is a medical device manufactured by Microlife Intellectual Property GmbH. It received FDA 510(k) clearance on 2017-07-20 under approval number K170219. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Microlife Digital Infrared Ear Thermometer?

Microlife Digital Infrared Ear Thermometer is a medical device that received FDA 510(k) clearance on 2017-07-20. It is manufactured by Microlife Intellectual Property GmbH. The 510(k) number is K170219.

When was Microlife Digital Infrared Ear Thermometer approved by the FDA?

Microlife Digital Infrared Ear Thermometer received FDA 510(k) clearance on 2017-07-20, under approval number K170219.

What company makes Microlife Digital Infrared Ear Thermometer?

Microlife Digital Infrared Ear Thermometer is manufactured by Microlife Intellectual Property GmbH.

What is the FDA product code for Microlife Digital Infrared Ear Thermometer?

The FDA product code for Microlife Digital Infrared Ear Thermometer is FLL.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.