免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据，仅供一般参考，不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

Plaxpot 多血浆

K号: K220493 · 2023-10-27

申请人Gcs Co. Limited
决定日期2023-10-27
产品代码QVJ
咨询委员会SU 请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同

器械摘要

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.

常见问题

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.

相关临床试验

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

NCT07608549FLASHPilot 1期安全性研究NOT_YET_RECRUITINGNCT06562205PAP系统外部临床研究（ECS）NOT_YET_RECRUITINGNCT06443177交感神经调节对动脉瘤性蛛网膜下腔出血继发脑动脉痉挛的影响SUSPENDEDNCT07095751人工智能辅助尿路摄像头评估系统，用于诊断膀胱癌NOT_YET_RECRUITING

相关器械（代码：QVJ）

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K233760Mjolnir Pro. (多电极等离子体)Shenzhen Leaflife Technology Co., Ltd.K213247JETT PLASMA Medical IICompex, Spol, S.R.O.K223440Plasma Pen (Plasma MD)；Plasma Pen (Plasma +)Plasma Concepts

官方来源

在 FDA 数据库中查看 →

数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。

↑