FDA 510(k)

Plaxpot Multi Plasma

K-Number: K220493 · 2023-10-27

Decision Date2023-10-27

Product CodeQVJ

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

Plaxpot Multi Plasma is the device name listed in this FDA 510(k) record. The listed applicant is Gcs Co. Limited. It received FDA 510(k) clearance on 2023-10-27 under 510(k) number K220493. 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 Plaxpot Multi Plasma?

Plaxpot Multi Plasma is a medical device that received FDA 510(k) clearance on 2023-10-27. The listed applicant is Gcs Co. Limited. The 510(k) number is K220493.

When did Plaxpot Multi Plasma receive FDA 510(k) clearance?

Plaxpot Multi Plasma received FDA 510(k) clearance on 2023-10-27, under 510(k) number K220493.

Who is the listed applicant for Plaxpot Multi Plasma?

The FDA 510(k) record lists Gcs Co. Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Plaxpot Multi Plasma?

The FDA product code for Plaxpot Multi Plasma is QVJ.

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.

K233760Mjolnir Pro. (Multi–electrode plasma)Shenzhen Leaflife Technology Co., Ltd.K213247JETT PLASMA Medical IICompex, Spol, S.R.O.K223440Plasma Pen (Plasma MD); Plasma Pen (Plasma +)Plasma Concepts

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.