FDA 510(k)

MOZI TPS

K-Number: K223724 · 2023-07-10

Decision Date2023-07-10

Product CodeMUJ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MOZI TPS is the device name listed in this FDA 510(k) record. The listed applicant is Manteia Technologies Co., Ltd.. It received FDA 510(k) clearance on 2023-07-10 under 510(k) 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. The listed applicant is Manteia Technologies Co., Ltd.. The 510(k) number is K223724.

When did MOZI TPS receive FDA 510(k) clearance?

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

Who is the listed applicant for MOZI TPS?

The FDA 510(k) record lists Manteia Technologies Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOZI TPS?

The FDA product code for MOZI TPS is MUJ.

Other records listing Manteia Technologies 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.

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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.