FDA 510(k)

StarFormer

K号: K234061 · 2024-07-01

决定日期2024-07-01

产品代码KPI

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决定实质等同

器械摘要

StarFormer is the device name listed in this FDA 510(k) record. The listed applicant is Fotona D.O.O.. It received FDA 510(k) clearance on 2024-07-01 under 510(k) number K234061. The device is classified under product code KPI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the StarFormer?

StarFormer is a medical device that received FDA 510(k) clearance on 2024-07-01. The listed applicant is Fotona D.O.O.. The 510(k) number is K234061.

When did StarFormer receive FDA 510(k) clearance?

StarFormer received FDA 510(k) clearance on 2024-07-01, under 510(k) number K234061.

Who is the listed applicant for StarFormer?

FDA 510(k)记录显示Fotona D.O.O.为申请人。这本身并不能确立该设备制造商的身份。

What is the FDA product code for StarFormer?

The FDA product code for StarFormer is KPI.

列明Fotona D.O.O.为申报人的其他记录

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。

K252723Dynamis Pro Family K241785StarFormer (M008-3T)K242202LightWalker激光系统家族 K221274StarFormer，TightWave K223540AvalancheLase家庭 K221712Fotona XPulse 激光系统家族 (XPulse 1064 nm, XPulse 810 nm, XPulse 980 nm)

查看所有 17 个设备 →

相关器械（代码：KPI）

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。

K262353BTL-299-FBTL Industries, Inc.K260178盆底肌肉训练器（KM510，KM516B）Shenzhen Konmed Technology Co., Ltd.K252601盆底肌肉训练器（PC22A）；盆底肌肉训练器（PC22A-L）；盆底肌肉训练器（PC22E）；盆底肌肉训练器（PC22E-L）Hunan Accurate Bio-Medical Technology Co., Ltd.K252552Pelvic Floor Rehabilitation Therapy Device (PD2301/PD2302/PD2303)Shenzhen Changkun Technology Co., Ltd.K252831Pelvic Floor Treatment Device (DLR-8920, DLR-8921, DLR-8922, DLR-8923, DLR-8924, DLR-8925, DLR-8926, DLR-8927)Dolanvy (Suzhou) Medical Technology Co., Ltd.K252334PELVIPOWER盆腔功能性磁刺激(PELVIPOWER盆腔FMS)(033-0-1100-02)Pontemedag

官方来源

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