FDA 510(k)

DIGITAL CLINICAL THERMOMETER, MODELS ST-8A3C AND ST-8A3F

K-Number: K042013 · 2004-09-08

Decision Date2004-09-08

Product CodeFLL

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

DIGITAL CLINICAL THERMOMETER, MODELS ST-8A3C AND ST-8A3F is the device name listed in this FDA 510(k) record. The listed applicant is Mesure Technology Co., Ltd.. It received FDA 510(k) clearance on 2004-09-08 under 510(k) number K042013. 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 DIGITAL CLINICAL THERMOMETER, MODELS ST-8A3C AND ST-8A3F?

DIGITAL CLINICAL THERMOMETER, MODELS ST-8A3C AND ST-8A3F is a medical device that received FDA 510(k) clearance on 2004-09-08. The listed applicant is Mesure Technology Co., Ltd.. The 510(k) number is K042013.

When did DIGITAL CLINICAL THERMOMETER, MODELS ST-8A3C AND ST-8A3F receive FDA 510(k) clearance?

DIGITAL CLINICAL THERMOMETER, MODELS ST-8A3C AND ST-8A3F received FDA 510(k) clearance on 2004-09-08, under 510(k) number K042013.

Who is the listed applicant for DIGITAL CLINICAL THERMOMETER, MODELS ST-8A3C AND ST-8A3F?

The FDA 510(k) record lists Mesure Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGITAL CLINICAL THERMOMETER, MODELS ST-8A3C AND ST-8A3F?

The FDA product code for DIGITAL CLINICAL THERMOMETER, MODELS ST-8A3C AND ST-8A3F is FLL.

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Other records listing Mesure Technology Co., Ltd. as applicant

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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.