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FDA 510(k)

WIRELESS TEMPERATURE MONITOR / MODELS ST323C AND ST323F.

K-Number: K063542 · 2007-04-10

Decision Date2007-04-10
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WIRELESS TEMPERATURE MONITOR / MODELS ST323C AND ST323F. is the device name listed in this FDA 510(k) record. The listed applicant is Mesure Technology Co., Ltd.. It received FDA 510(k) clearance on 2007-04-10 under 510(k) number K063542. 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 WIRELESS TEMPERATURE MONITOR / MODELS ST323C AND ST323F.?

WIRELESS TEMPERATURE MONITOR / MODELS ST323C AND ST323F. is a medical device that received FDA 510(k) clearance on 2007-04-10. The listed applicant is Mesure Technology Co., Ltd.. The 510(k) number is K063542.

When did WIRELESS TEMPERATURE MONITOR / MODELS ST323C AND ST323F. receive FDA 510(k) clearance?

WIRELESS TEMPERATURE MONITOR / MODELS ST323C AND ST323F. received FDA 510(k) clearance on 2007-04-10, under 510(k) number K063542.

Who is the listed applicant for WIRELESS TEMPERATURE MONITOR / MODELS ST323C AND ST323F.?

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 WIRELESS TEMPERATURE MONITOR / MODELS ST323C AND ST323F.?

The FDA product code for WIRELESS TEMPERATURE MONITOR / MODELS ST323C AND ST323F. 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.

View all 8 devices →

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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