FDA 510(k)

Neurophet AQUA (V3.1)

K号: K242215 · 2024-10-25

决定日期2024-10-25

产品代码QIH

咨询委员会RA

决定实质等同

器械摘要

Neurophet AQUA (V3.1) is the device name listed in this FDA 510(k) record. The listed applicant is Neurophet., Inc.. It received FDA 510(k) clearance on 2024-10-25 under 510(k) number K242215. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Neurophet AQUA (V3.1)?

Neurophet AQUA (V3.1) is a medical device that received FDA 510(k) clearance on 2024-10-25. The listed applicant is Neurophet., Inc.. The 510(k) number is K242215.

When did Neurophet AQUA (V3.1) receive FDA 510(k) clearance?

Neurophet AQUA (V3.1) received FDA 510(k) clearance on 2024-10-25, under 510(k) number K242215.

Who is the listed applicant for Neurophet AQUA (V3.1)?

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

What is the FDA product code for Neurophet AQUA (V3.1)?

The FDA product code for Neurophet AQUA (V3.1) is QIH.

列明Neurophet., 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。

K252563Neurophet SCALE PET K261273Neurophet AQUA K252496Neurophet AQUA AD Plus K220437Neurophet AQUA K221405Neurophet SCALE PET

官方来源

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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。