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FDA 510(k)

BloodSTOP iX Trauma Matrix (TM-iX-20)

K号: K253017 · 2026-04-30

决定日期2026-04-30
产品代码QSY
决定实质等同

器械摘要

BloodSTOP iX Trauma Matrix (TM-iX-20) is the device name listed in this FDA 510(k) record. The listed applicant is Lifescience Plus, Inc.. It received FDA 510(k) clearance on 2026-04-30 under 510(k) number K253017. The device is classified under product code QSY. FDA Decision: Substantially Equivalent.

常见问题

What is the BloodSTOP iX Trauma Matrix (TM-iX-20)?

BloodSTOP iX Trauma Matrix (TM-iX-20) is a medical device that received FDA 510(k) clearance on 2026-04-30. The listed applicant is Lifescience Plus, Inc.. The 510(k) number is K253017.

When did BloodSTOP iX Trauma Matrix (TM-iX-20) receive FDA 510(k) clearance?

BloodSTOP iX Trauma Matrix (TM-iX-20) received FDA 510(k) clearance on 2026-04-30, under 510(k) number K253017.

Who is the listed applicant for BloodSTOP iX Trauma Matrix (TM-iX-20)?

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

What is the FDA product code for BloodSTOP iX Trauma Matrix (TM-iX-20)?

The FDA product code for BloodSTOP iX Trauma Matrix (TM-iX-20) is QSY.

相关临床试验

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列明Lifescience Plus, Inc.为申报人的其他记录

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相关器械(代码:QSY)

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

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