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FDA 510(k)

FAST THERMOMETER MODELS ST713C AND ST713F

K-Number: K011585 · 2001-06-13

Decision Date2001-06-13
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FAST THERMOMETER MODELS ST713C AND ST713F is the device name listed in this FDA 510(k) record. The listed applicant is Mesure Technology. It received FDA 510(k) clearance on 2001-06-13 under 510(k) number K011585. 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 FAST THERMOMETER MODELS ST713C AND ST713F?

FAST THERMOMETER MODELS ST713C AND ST713F is a medical device that received FDA 510(k) clearance on 2001-06-13. The listed applicant is Mesure Technology. The 510(k) number is K011585.

When did FAST THERMOMETER MODELS ST713C AND ST713F receive FDA 510(k) clearance?

FAST THERMOMETER MODELS ST713C AND ST713F received FDA 510(k) clearance on 2001-06-13, under 510(k) number K011585.

Who is the listed applicant for FAST THERMOMETER MODELS ST713C AND ST713F?

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 FAST THERMOMETER MODELS ST713C AND ST713F?

The FDA product code for FAST THERMOMETER MODELS ST713C AND ST713F 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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