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FDA 510(k)

MOZI TPS

K-Number: K223724 · 2023-07-10

ApplicantManteia Technologies Co., Ltd.
Decision Date2023-07-10
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MOZI TPS is a medical device manufactured by Manteia Technologies Co., Ltd.. It received FDA 510(k) clearance on 2023-07-10 under approval number K223724. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOZI TPS?

MOZI TPS is a medical device that received FDA 510(k) clearance on 2023-07-10. It is manufactured by Manteia Technologies Co., Ltd.. The 510(k) number is K223724.

When was MOZI TPS approved by the FDA?

MOZI TPS received FDA 510(k) clearance on 2023-07-10, under approval number K223724.

What company makes MOZI TPS?

MOZI TPS is manufactured by Manteia Technologies Co., Ltd..

What is the FDA product code for MOZI TPS?

The FDA product code for MOZI TPS is MUJ.

Other Devices by Manteia Technologies Co., Ltd.

K223834AccuCheck K221706AccuContour K250780ARTAssistant K250696AccuCheck K251351AccuContour 4.0

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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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