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FDA 510(k)

SHAKER DIGITAL THERMOMETER

K-Number: K112703 · 2011-10-04

ApplicantMeasure Technology Co. , Ltd.
Decision Date2011-10-04
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHAKER DIGITAL THERMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Measure Technology Co. , Ltd.. It received FDA 510(k) clearance on 2011-10-04 under 510(k) number K112703. 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 SHAKER DIGITAL THERMOMETER?

SHAKER DIGITAL THERMOMETER is a medical device that received FDA 510(k) clearance on 2011-10-04. The listed applicant is Measure Technology Co. , Ltd.. The 510(k) number is K112703.

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

SHAKER DIGITAL THERMOMETER received FDA 510(k) clearance on 2011-10-04, under 510(k) number K112703.

Who is the listed applicant for SHAKER DIGITAL THERMOMETER?

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

What is the FDA product code for SHAKER DIGITAL THERMOMETER?

The FDA product code for SHAKER DIGITAL THERMOMETER is FLL.

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Related Devices (Code: FLL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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