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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 the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Leaflife Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-02-20 under 510(k) 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. The listed applicant is Shenzhen Leaflife Technology Co., Ltd.. The 510(k) number is K233760.

When did Mjolnir Pro. (Multi–electrode plasma) receive FDA 510(k) clearance?

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

Who is the listed applicant for Mjolnir Pro. (Multi–electrode plasma)?

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

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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Related Devices (Code: QVJ)

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

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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