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FDA 510(k)

DIGITAL CLINICAL THERMOMETER ST-813A, ST-814A, ST-823 AND ST-823A

K-Number: K962520 · 1996-09-12

Decision Date1996-09-12
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DIGITAL CLINICAL THERMOMETER ST-813A, ST-814A, ST-823 AND ST-823A is the device name listed in this FDA 510(k) record. The listed applicant is Mesure Technology. It received FDA 510(k) clearance on 1996-09-12 under 510(k) number K962520. 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 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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