INDIGO Aspiration System (CAT RX Aspiration Catheter and Separator 4)
K号: K220683 · 2022-10-04
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器械摘要
常见问题
What is the INDIGO Aspiration System (CAT RX Aspiration Catheter and Separator 4)?
INDIGO Aspiration System (CAT RX Aspiration Catheter and Separator 4) is a medical device that received FDA 510(k) clearance on 2022-10-04. The listed applicant is Penumbra, Inc.. The 510(k) number is K220683.
When did INDIGO Aspiration System (CAT RX Aspiration Catheter and Separator 4) receive FDA 510(k) clearance?
INDIGO Aspiration System (CAT RX Aspiration Catheter and Separator 4) received FDA 510(k) clearance on 2022-10-04, under 510(k) number K220683.
Who is the listed applicant for INDIGO Aspiration System (CAT RX Aspiration Catheter and Separator 4)?
The FDA 510(k) record lists Penumbra, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INDIGO Aspiration System (CAT RX Aspiration Catheter and Separator 4)?
The FDA product code for INDIGO Aspiration System (CAT RX Aspiration Catheter and Separator 4) is QEW.
相关临床试验
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列明Penumbra, Inc.为申报人的其他记录
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:QEW)
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
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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