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FDA 510(k)

RESPONDER 多糖止血剂

K号: K220525 · 2023-12-04

决定日期2023-12-04
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 2023-12-04 under 510(k) number K220525. 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 2023-12-04. The listed applicant is Starch Medical, Inc.. The 510(k) number is K220525.

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

RESPONDER Polysaccharide Hemostat received FDA 510(k) clearance on 2023-12-04, under 510(k) number K220525.

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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