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FDA 510(k)

MICROLIFE DIGITAL ELECTRONIC THERMOMETER, MODEL MT16K1

K-Number: K091589 · 2009-06-10

ApplicantMicrolife Intellectual Property GmbH
Decision Date2009-06-10
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MICROLIFE DIGITAL ELECTRONIC THERMOMETER, MODEL MT16K1 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 2009-06-10 under 510(k) number K091589. 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 ELECTRONIC THERMOMETER, MODEL MT16K1?

MICROLIFE DIGITAL ELECTRONIC THERMOMETER, MODEL MT16K1 is a medical device that received FDA 510(k) clearance on 2009-06-10. The listed applicant is Microlife Intellectual Property GmbH. The 510(k) number is K091589.

When did MICROLIFE DIGITAL ELECTRONIC THERMOMETER, MODEL MT16K1 receive FDA 510(k) clearance?

MICROLIFE DIGITAL ELECTRONIC THERMOMETER, MODEL MT16K1 received FDA 510(k) clearance on 2009-06-10, under 510(k) number K091589.

Who is the listed applicant for MICROLIFE DIGITAL ELECTRONIC THERMOMETER, MODEL MT16K1?

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 ELECTRONIC THERMOMETER, MODEL MT16K1?

The FDA product code for MICROLIFE DIGITAL ELECTRONIC THERMOMETER, MODEL MT16K1 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.

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