Vascette HP（止血垫）
K号: K220566 · 2022-07-29
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器械摘要
Vascette HP (hemostatic pad) is the device name listed in this FDA 510(k) record. The listed applicant is Koag, LLC. It received FDA 510(k) clearance on 2022-07-29 under 510(k) number K220566. The device is classified under product code QSY. FDA Decision: Substantially Equivalent.
常见问题
What is the Vascette HP (hemostatic pad)?
Vascette HP (hemostatic pad) is a medical device that received FDA 510(k) clearance on 2022-07-29. The listed applicant is Koag, LLC. The 510(k) number is K220566.
When did Vascette HP (hemostatic pad) receive FDA 510(k) clearance?
Vascette HP (hemostatic pad) received FDA 510(k) clearance on 2022-07-29, under 510(k) number K220566.
Who is the listed applicant for Vascette HP (hemostatic pad)?
The FDA 510(k) record lists Koag, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vascette HP (hemostatic pad)?
The FDA product code for Vascette HP (hemostatic pad) is QSY.
相关临床试验
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。
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。
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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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