DIGITAL CLINICAL THERMOMETER ST-813A, ST-814A, ST-823 AND ST-823A
K-Number: K962520 · 1996-09-12
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Device Summary
Frequently Asked Questions
What is the DIGITAL CLINICAL THERMOMETER ST-813A, ST-814A, ST-823 AND ST-823A?
DIGITAL CLINICAL THERMOMETER ST-813A, ST-814A, ST-823 AND ST-823A is a medical device that received FDA 510(k) clearance on 1996-09-12. The listed applicant is Mesure Technology. The 510(k) number is K962520.
When did DIGITAL CLINICAL THERMOMETER ST-813A, ST-814A, ST-823 AND ST-823A receive FDA 510(k) clearance?
DIGITAL CLINICAL THERMOMETER ST-813A, ST-814A, ST-823 AND ST-823A received FDA 510(k) clearance on 1996-09-12, under 510(k) number K962520.
Who is the listed applicant for DIGITAL CLINICAL THERMOMETER ST-813A, ST-814A, ST-823 AND ST-823A?
The FDA 510(k) record lists Mesure Technology as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIGITAL CLINICAL THERMOMETER ST-813A, ST-814A, ST-823 AND ST-823A?
The FDA product code for DIGITAL CLINICAL THERMOMETER ST-813A, ST-814A, ST-823 AND ST-823A 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 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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