FDA 510(k)

MICROLIFE DIGITAL UNDERARM THERMOMETER

K-Number: K103680 · 2011-04-06

ApplicantMicrolife Intellectual Property GmbH

Decision Date2011-04-06

Product CodeFLL

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

MICROLIFE DIGITAL UNDERARM 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 2011-04-06 under 510(k) number K103680. 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 UNDERARM THERMOMETER?

MICROLIFE DIGITAL UNDERARM THERMOMETER is a medical device that received FDA 510(k) clearance on 2011-04-06. The listed applicant is Microlife Intellectual Property GmbH. The 510(k) number is K103680.

When did MICROLIFE DIGITAL UNDERARM THERMOMETER receive FDA 510(k) clearance?

MICROLIFE DIGITAL UNDERARM THERMOMETER received FDA 510(k) clearance on 2011-04-06, under 510(k) number K103680.

Who is the listed applicant for MICROLIFE DIGITAL UNDERARM 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 DIGITAL UNDERARM THERMOMETER?

The FDA product code for MICROLIFE DIGITAL UNDERARM THERMOMETER is FLL.

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Related Devices (Code: 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.