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FDA 510(k)

MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL QT1JC1

K-Number: K062867 · 2006-12-06

ApplicantMicrolife Intellectual Property GmbH
Decision Date2006-12-06
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL QT1JC1 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 2006-12-06 under 510(k) number K062867. 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 INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL QT1JC1?

MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL QT1JC1 is a medical device that received FDA 510(k) clearance on 2006-12-06. The listed applicant is Microlife Intellectual Property GmbH. The 510(k) number is K062867.

When did MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL QT1JC1 receive FDA 510(k) clearance?

MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL QT1JC1 received FDA 510(k) clearance on 2006-12-06, under 510(k) number K062867.

Who is the listed applicant for MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL QT1JC1?

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 INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL QT1JC1?

The FDA product code for MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL QT1JC1 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.

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