QSCHECK UISACR
K号: K252619 · 2026-02-20
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申请人Qstag, Inc.
决定日期2026-02-20
产品代码JFY
咨询委员会CH
请注意，您提供的文本“CH”不足以进行翻译。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
QSCHECK UISACR is the device name listed in this FDA 510(k) record. The listed applicant is Qstag, Inc.. It received FDA 510(k) clearance on 2026-02-20 under 510(k) number K252619. The device is classified under product code JFY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the QSCHECK UISACR?
QSCHECK UISACR is a medical device that received FDA 510(k) clearance on 2026-02-20. The listed applicant is Qstag, Inc.. The 510(k) number is K252619.
When did QSCHECK UISACR receive FDA 510(k) clearance?
QSCHECK UISACR received FDA 510(k) clearance on 2026-02-20, under 510(k) number K252619.
Who is the listed applicant for QSCHECK UISACR?
The FDA 510(k) record lists Qstag, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QSCHECK UISACR?
The FDA product code for QSCHECK UISACR is JFY.
相关临床试验
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相关器械（代码：JFY）
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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