负压伤口治疗设备（V-Move，V-Grand）
K号: K241023 · 2024-08-19
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器械摘要
Negative Pressure Wound Therapy Device (V-Move, V-Grand) is the device name listed in this FDA 510(k) record. The listed applicant is Med Way, Inc.. It received FDA 510(k) clearance on 2024-08-19 under 510(k) number K241023. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Negative Pressure Wound Therapy Device (V-Move, V-Grand)?
Negative Pressure Wound Therapy Device (V-Move, V-Grand) is a medical device that received FDA 510(k) clearance on 2024-08-19. The listed applicant is Med Way, Inc.. The 510(k) number is K241023.
When did Negative Pressure Wound Therapy Device (V-Move, V-Grand) receive FDA 510(k) clearance?
Negative Pressure Wound Therapy Device (V-Move, V-Grand) received FDA 510(k) clearance on 2024-08-19, under 510(k) number K241023.
Who is the listed applicant for Negative Pressure Wound Therapy Device (V-Move, V-Grand)?
The FDA 510(k) record lists Med Way, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Negative Pressure Wound Therapy Device (V-Move, V-Grand)?
The FDA product code for Negative Pressure Wound Therapy Device (V-Move, V-Grand) is OMP.
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。
相关器械（代码：OMP）
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。
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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。
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