FDA 510(k)

Microlife Non-Contact Infrared Forehead Thermometer

Numéro K : K191829 · 2020-02-13

DemandeurMicrolife Intellectual Property GmbH

Date de décision2020-02-13

Code produitFLL

Comité consultatifHO

DécisionSubstantially Equivalent

Résumé du dispositif

Microlife Non-Contact Infrared Forehead Thermometer is the device name listed in this FDA 510(k) record. The listed applicant is Microlife Intellectual Property GmbH. It received FDA 510(k) clearance on 2020-02-13 under 510(k) number K191829. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the Microlife Non-Contact Infrared Forehead Thermometer?

Microlife Non-Contact Infrared Forehead Thermometer is a medical device that received FDA 510(k) clearance on 2020-02-13. The listed applicant is Microlife Intellectual Property GmbH. The 510(k) number is K191829.

When did Microlife Non-Contact Infrared Forehead Thermometer receive FDA 510(k) clearance?

Microlife Non-Contact Infrared Forehead Thermometer received FDA 510(k) clearance on 2020-02-13, under 510(k) number K191829.

Who is the listed applicant for Microlife Non-Contact Infrared Forehead Thermometer?

The FDA 510(k) record lists Microlife Intellectual Property GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Microlife Non-Contact Infrared Forehead Thermometer?

The FDA product code for Microlife Non-Contact Infrared Forehead Thermometer is FLL.

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Dispositifs connexes (Code : FLL)

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Source officielle

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