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FDA 510(k)

Radio Frequency Plasma Surgical Systems; Radio Frequency Plasma Surgical Electrodes

K-Number: K221743 · 2023-09-07

ApplicantJiangsu Bonss Medical Technology Co., Ltd.
Decision Date2023-09-07
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Radio Frequency Plasma Surgical Systems; Radio Frequency Plasma Surgical Electrodes is a medical device manufactured by Jiangsu Bonss Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-09-07 under approval number K221743. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Radio Frequency Plasma Surgical Systems; Radio Frequency Plasma Surgical Electrodes?

Radio Frequency Plasma Surgical Systems; Radio Frequency Plasma Surgical Electrodes is a medical device that received FDA 510(k) clearance on 2023-09-07. It is manufactured by Jiangsu Bonss Medical Technology Co., Ltd.. The 510(k) number is K221743.

When was Radio Frequency Plasma Surgical Systems; Radio Frequency Plasma Surgical Electrodes approved by the FDA?

Radio Frequency Plasma Surgical Systems; Radio Frequency Plasma Surgical Electrodes received FDA 510(k) clearance on 2023-09-07, under approval number K221743.

What company makes Radio Frequency Plasma Surgical Systems; Radio Frequency Plasma Surgical Electrodes?

Radio Frequency Plasma Surgical Systems; Radio Frequency Plasma Surgical Electrodes is manufactured by Jiangsu Bonss Medical Technology Co., Ltd..

What is the FDA product code for Radio Frequency Plasma Surgical Systems; Radio Frequency Plasma Surgical Electrodes?

The FDA product code for Radio Frequency Plasma Surgical Systems; Radio Frequency Plasma Surgical Electrodes is GEI.

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Related PubMed Literature

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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.

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