Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

EASYTEM DUO, FOREHEAD/EAR THERMOMETER, MODEL BT-021

K-Number: K033077 · 2004-04-30

Decision Date2004-04-30
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EASYTEM DUO, FOREHEAD/EAR THERMOMETER, MODEL BT-021 is the device name listed in this FDA 510(k) record. The listed applicant is Metatech Co., Ltd.. It received FDA 510(k) clearance on 2004-04-30 under 510(k) number K033077. 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 EASYTEM DUO, FOREHEAD/EAR THERMOMETER, MODEL BT-021?

EASYTEM DUO, FOREHEAD/EAR THERMOMETER, MODEL BT-021 is a medical device that received FDA 510(k) clearance on 2004-04-30. The listed applicant is Metatech Co., Ltd.. The 510(k) number is K033077.

When did EASYTEM DUO, FOREHEAD/EAR THERMOMETER, MODEL BT-021 receive FDA 510(k) clearance?

EASYTEM DUO, FOREHEAD/EAR THERMOMETER, MODEL BT-021 received FDA 510(k) clearance on 2004-04-30, under 510(k) number K033077.

Who is the listed applicant for EASYTEM DUO, FOREHEAD/EAR THERMOMETER, MODEL BT-021?

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

What is the FDA product code for EASYTEM DUO, FOREHEAD/EAR THERMOMETER, MODEL BT-021?

The FDA product code for EASYTEM DUO, FOREHEAD/EAR THERMOMETER, MODEL BT-021 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 Metatech Co., 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.

↑