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FDA 510(k)

Mjolnir Pro. (Multi–electrode plasma)

K-Number: K233760 · 2024-02-20

ApplicantShenzhen Leaflife Technology Co., Ltd.
Decision Date2024-02-20
Product CodeQVJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Mjolnir Pro. (Multi–electrode plasma) is a medical device manufactured by Shenzhen Leaflife Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-02-20 under approval number K233760. The device is classified under product code QVJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Mjolnir Pro. (Multi–electrode plasma)?

Mjolnir Pro. (Multi–electrode plasma) is a medical device that received FDA 510(k) clearance on 2024-02-20. It is manufactured by Shenzhen Leaflife Technology Co., Ltd.. The 510(k) number is K233760.

When was Mjolnir Pro. (Multi–electrode plasma) approved by the FDA?

Mjolnir Pro. (Multi–electrode plasma) received FDA 510(k) clearance on 2024-02-20, under approval number K233760.

What company makes Mjolnir Pro. (Multi–electrode plasma)?

Mjolnir Pro. (Multi–electrode plasma) is manufactured by Shenzhen Leaflife Technology Co., Ltd..

What is the FDA product code for Mjolnir Pro. (Multi–electrode plasma)?

The FDA product code for Mjolnir Pro. (Multi–electrode plasma) is QVJ.

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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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