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FDA 510(k)

MICROLIFE DIGITAL BASAL THERMOMETER, MODEL MT 1921

K-Number: K030961 · 2003-09-12

ApplicantMicrolife Corp.
Decision Date2003-09-12
Product CodeLHD
DecisionSubstantially Equivalent

Device Summary

MICROLIFE DIGITAL BASAL THERMOMETER, MODEL MT 1921 is the device name listed in this FDA 510(k) record. The listed applicant is Microlife Corp.. It received FDA 510(k) clearance on 2003-09-12 under 510(k) number K030961. The device is classified under product code LHD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROLIFE DIGITAL BASAL THERMOMETER, MODEL MT 1921?

MICROLIFE DIGITAL BASAL THERMOMETER, MODEL MT 1921 is a medical device that received FDA 510(k) clearance on 2003-09-12. The listed applicant is Microlife Corp.. The 510(k) number is K030961.

When did MICROLIFE DIGITAL BASAL THERMOMETER, MODEL MT 1921 receive FDA 510(k) clearance?

MICROLIFE DIGITAL BASAL THERMOMETER, MODEL MT 1921 received FDA 510(k) clearance on 2003-09-12, under 510(k) number K030961.

Who is the listed applicant for MICROLIFE DIGITAL BASAL THERMOMETER, MODEL MT 1921?

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

What is the FDA product code for MICROLIFE DIGITAL BASAL THERMOMETER, MODEL MT 1921?

The FDA product code for MICROLIFE DIGITAL BASAL THERMOMETER, MODEL MT 1921 is LHD.

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Official Source

View on FDA Database →

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

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