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FDA 510(k)

Bondiloxs 表面止血颗粒

K号: K161274 · 2017-01-18

决定日期2017-01-18
产品代码QSY
决定实质等同

器械摘要

Bondiloxs Topical Hemostatic Granules is the device name listed in this FDA 510(k) record. The listed applicant is Medtrade Products , Ltd.. It received FDA 510(k) clearance on 2017-01-18 under 510(k) number K161274. The device is classified under product code QSY. FDA Decision: Substantially Equivalent.

常见问题

What is the Bondiloxs Topical Hemostatic Granules?

Bondiloxs Topical Hemostatic Granules is a medical device that received FDA 510(k) clearance on 2017-01-18. The listed applicant is Medtrade Products , Ltd.. The 510(k) number is K161274.

When did Bondiloxs Topical Hemostatic Granules receive FDA 510(k) clearance?

Bondiloxs Topical Hemostatic Granules received FDA 510(k) clearance on 2017-01-18, under 510(k) number K161274.

Who is the listed applicant for Bondiloxs Topical Hemostatic Granules?

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

What is the FDA product code for Bondiloxs Topical Hemostatic Granules?

The FDA product code for Bondiloxs Topical Hemostatic Granules is QSY.

相关临床试验

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列明Medtrade Products , Ltd.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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