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FDA 510(k)

RESPONDER® 多糖止血剂

K号: K240454 · 2024-03-15

决定日期2024-03-15
产品代码QSY
决定实质等同

器械摘要

RESPONDER® Polysaccharide Hemostat is the device name listed in this FDA 510(k) record. The listed applicant is Starch Medical, Inc.. It received FDA 510(k) clearance on 2024-03-15 under 510(k) number K240454. The device is classified under product code QSY. FDA Decision: Substantially Equivalent.

常见问题

What is the RESPONDER® Polysaccharide Hemostat?

RESPONDER® Polysaccharide Hemostat is a medical device that received FDA 510(k) clearance on 2024-03-15. The listed applicant is Starch Medical, Inc.. The 510(k) number is K240454.

When did RESPONDER® Polysaccharide Hemostat receive FDA 510(k) clearance?

RESPONDER® Polysaccharide Hemostat received FDA 510(k) clearance on 2024-03-15, under 510(k) number K240454.

Who is the listed applicant for RESPONDER® Polysaccharide Hemostat?

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

What is the FDA product code for RESPONDER® Polysaccharide Hemostat?

The FDA product code for RESPONDER® Polysaccharide Hemostat is QSY.

相关临床试验

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列明Starch Medical, 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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