DIGITAL CLINICAL THERMOMETER/MODELS ST8C SERIES
K-Number: K071019 · 2007-04-27
Advertisement
Device Summary
Frequently Asked Questions
What is the DIGITAL CLINICAL THERMOMETER/MODELS ST8C SERIES?
DIGITAL CLINICAL THERMOMETER/MODELS ST8C SERIES is a medical device that received FDA 510(k) clearance on 2007-04-27. The listed applicant is Mesure Technology Co., Ltd.. The 510(k) number is K071019.
When did DIGITAL CLINICAL THERMOMETER/MODELS ST8C SERIES receive FDA 510(k) clearance?
DIGITAL CLINICAL THERMOMETER/MODELS ST8C SERIES received FDA 510(k) clearance on 2007-04-27, under 510(k) number K071019.
Who is the listed applicant for DIGITAL CLINICAL THERMOMETER/MODELS ST8C SERIES?
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 ST8C SERIES?
The FDA product code for DIGITAL CLINICAL THERMOMETER/MODELS ST8C 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 Mesure Technology 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.
Advertisement