FDA 510(k)

RelieVRx (Pico G3)

K号: K251519 · 2025-08-13

决定日期2025-08-13

产品代码QRA

咨询委员会NE 请注意，您提供的文本“NE”不足以进行翻译，因为它不是一个完整的句子或描述。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。

决定实质等同

器械摘要

RelieVRx (Pico G3) is the device name listed in this FDA 510(k) record. The listed applicant is Appliedvr. It received FDA 510(k) clearance on 2025-08-13 under 510(k) number K251519. The device is classified under product code QRA. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the RelieVRx (Pico G3)?

RelieVRx (Pico G3) is a medical device that received FDA 510(k) clearance on 2025-08-13. The listed applicant is Appliedvr. The 510(k) number is K251519.

When did RelieVRx (Pico G3) receive FDA 510(k) clearance?

RelieVRx (Pico G3) received FDA 510(k) clearance on 2025-08-13, under 510(k) number K251519.

Who is the listed applicant for RelieVRx (Pico G3)?

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

What is the FDA product code for RelieVRx (Pico G3)?

The FDA product code for RelieVRx (Pico G3) is QRA.

列明Appliedvr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。

K243417RelieVRx

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。