FDA 510(k)

光疗系统 (DUV-COMBO)

K号: K254234 · 2026-05-01

决定日期2026-05-01

产品代码FTC

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决定实质等同

器械摘要

Phototherapy System (DUV-COMBO) is the device name listed in this FDA 510(k) record. The listed applicant is Choyang Medics Co., Ltd.. It received FDA 510(k) clearance on 2026-05-01 under 510(k) number K254234. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Phototherapy System (DUV-COMBO)?

Phototherapy System (DUV-COMBO) is a medical device that received FDA 510(k) clearance on 2026-05-01. The listed applicant is Choyang Medics Co., Ltd.. The 510(k) number is K254234.

When did Phototherapy System (DUV-COMBO) receive FDA 510(k) clearance?

Phototherapy System (DUV-COMBO) received FDA 510(k) clearance on 2026-05-01, under 510(k) number K254234.

Who is the listed applicant for Phototherapy System (DUV-COMBO)?

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

What is the FDA product code for Phototherapy System (DUV-COMBO)?

The FDA product code for Phototherapy System (DUV-COMBO) is FTC.

相关器械（代码：FTC）

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。

K253871Klär Lite（RCW-KL1000）Radcliffe Watts, LLC K250425紫外线光疗设备APK Technology Co., Ltd.K244022308nm紫外线光疗系统（UV-K）；308nm紫外线光疗系统（UV-X）；308nm紫外线光疗系统（UV-Y）；308nm紫外线光疗系统（UV-Z）Boston Aesthetics, Inc.K242977308nm准分子光疗设备（CN-308E，KN-4003B3，KN-4003B4，KN-5000C KN-5000D，KN-5000H，KN-5000K）Xuzhou Kernel Medical Equipment Co., Ltd.K242908紫外线光疗设备（A组：SQ308PCHFD，SQ308PCQFD，SQ308PCPFD，SQ308PCNFD，SQ308PCMFD）；紫外线光疗设备（B组：SQ308PHTFF，SQ308PHSFF，SQ308PHRFF，SQ308PHZFG，SQ308PPUFF，SQ308PPVFF，SQ308PPWFG）Shanghai Sigma High-Tech Co., Ltd.K233811DT 控制光疗设备Daavlin Distributing Co.

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器械摘要

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相关器械（代码：FTC）

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