FDA 510(k)

伤口治疗系统（VHT-200）

K号: K250188 · 2025-03-10

决定日期2025-03-10

产品代码KPJ

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决定实质等同

器械摘要

Wound Treatment System (VHT-200) is the device name listed in this FDA 510(k) record. The listed applicant is Vaporox, Inc.. It received FDA 510(k) clearance on 2025-03-10 under 510(k) number K250188. The device is classified under product code KPJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Wound Treatment System (VHT-200)?

Wound Treatment System (VHT-200) is a medical device that received FDA 510(k) clearance on 2025-03-10. The listed applicant is Vaporox, Inc.. The 510(k) number is K250188.

When did Wound Treatment System (VHT-200) receive FDA 510(k) clearance?

Wound Treatment System (VHT-200) received FDA 510(k) clearance on 2025-03-10, under 510(k) number K250188.

Who is the listed applicant for Wound Treatment System (VHT-200)?

The FDA 510(k) record lists Vaporox, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Wound Treatment System (VHT-200)?

The FDA product code for Wound Treatment System (VHT-200) is KPJ.

列明Vaporox, Inc.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。

K212121VHT-200 创面治疗系统

官方来源

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