Integrity V500 (Integrity, Integrity with VEMP)
K号: K242954 · 2024-12-19
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决定日期2024-12-19
产品代码GWJ
咨询委员会NE
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器械摘要
Integrity V500 (Integrity, Integrity with VEMP) is the device name listed in this FDA 510(k) record. The listed applicant is Vivosonic, Inc.. It received FDA 510(k) clearance on 2024-12-19 under 510(k) number K242954. The device is classified under product code GWJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Integrity V500 (Integrity, Integrity with VEMP)?
Integrity V500 (Integrity, Integrity with VEMP) is a medical device that received FDA 510(k) clearance on 2024-12-19. The listed applicant is Vivosonic, Inc.. The 510(k) number is K242954.
When did Integrity V500 (Integrity, Integrity with VEMP) receive FDA 510(k) clearance?
Integrity V500 (Integrity, Integrity with VEMP) received FDA 510(k) clearance on 2024-12-19, under 510(k) number K242954.
Who is the listed applicant for Integrity V500 (Integrity, Integrity with VEMP)?
The FDA 510(k) record lists Vivosonic, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Integrity V500 (Integrity, Integrity with VEMP)?
The FDA product code for Integrity V500 (Integrity, Integrity with VEMP) is GWJ.
相关临床试验
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相关器械（代码：GWJ）
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。
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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