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FDA 510(k)

MODEL GT980201 ELECTRONIC THERMOMETER

K-Number: K021028 · 2002-04-08

Decision Date2002-04-08
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL GT980201 ELECTRONIC THERMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Global Treasure , Ltd.. It received FDA 510(k) clearance on 2002-04-08 under 510(k) number K021028. 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 MODEL GT980201 ELECTRONIC THERMOMETER?

MODEL GT980201 ELECTRONIC THERMOMETER is a medical device that received FDA 510(k) clearance on 2002-04-08. The listed applicant is Global Treasure , Ltd.. The 510(k) number is K021028.

When did MODEL GT980201 ELECTRONIC THERMOMETER receive FDA 510(k) clearance?

MODEL GT980201 ELECTRONIC THERMOMETER received FDA 510(k) clearance on 2002-04-08, under 510(k) number K021028.

Who is the listed applicant for MODEL GT980201 ELECTRONIC THERMOMETER?

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

What is the FDA product code for MODEL GT980201 ELECTRONIC THERMOMETER?

The FDA product code for MODEL GT980201 ELECTRONIC THERMOMETER is FLL.

Related Clinical Trials

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.

Other records listing Global Treasure , Ltd. as applicant

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.

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.

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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