HIVOX EAR THERMOMETER, TS SERIES
K-Number: K020471 · 2002-05-02
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Device Summary
Frequently Asked Questions
What is the HIVOX EAR THERMOMETER, TS SERIES?
HIVOX EAR THERMOMETER, TS SERIES is a medical device that received FDA 510(k) clearance on 2002-05-02. The listed applicant is Hivox Biotek, Inc.. The 510(k) number is K020471.
When did HIVOX EAR THERMOMETER, TS SERIES receive FDA 510(k) clearance?
HIVOX EAR THERMOMETER, TS SERIES received FDA 510(k) clearance on 2002-05-02, under 510(k) number K020471.
Who is the listed applicant for HIVOX EAR THERMOMETER, TS SERIES?
The FDA 510(k) record lists Hivox Biotek, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HIVOX EAR THERMOMETER, TS SERIES?
The FDA product code for HIVOX EAR THERMOMETER, TS SERIES 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 Hivox Biotek, Inc. 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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