FDA 510(k)

Neurophet SCALE PET

K号: K252563 · 2026-05-15

决定日期2026-05-15

产品代码QIH

咨询委员会RA

决定实质等同

器械摘要

Neurophet SCALE PET is the device name listed in this FDA 510(k) record. The listed applicant is Neurophet., Inc.. It received FDA 510(k) clearance on 2026-05-15 under 510(k) number K252563. 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 SCALE PET?

Neurophet SCALE PET is a medical device that received FDA 510(k) clearance on 2026-05-15. The listed applicant is Neurophet., Inc.. The 510(k) number is K252563.

When did Neurophet SCALE PET receive FDA 510(k) clearance?

Neurophet SCALE PET received FDA 510(k) clearance on 2026-05-15, under 510(k) number K252563.

Who is the listed applicant for Neurophet SCALE PET?

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 SCALE PET?

The FDA product code for Neurophet SCALE PET 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。

K261273Neurophet AQUA K252496Neurophet AQUA AD Plus K242215Neurophet AQUA (V3.1)K220437Neurophet AQUA K221405Neurophet SCALE PET

官方来源

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