Kahook双刀片滑行（KDB滑行）
K号: K220891 · 2024-05-17
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决定日期2024-05-17
产品代码QUQ
咨询委员会SU
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器械摘要
Kahook Dual Blade Glide (KDB Glide) is the device name listed in this FDA 510(k) record. The listed applicant is New World Medical, Inc.. It received FDA 510(k) clearance on 2024-05-17 under 510(k) number K220891. The device is classified under product code QUQ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Kahook Dual Blade Glide (KDB Glide)?
Kahook Dual Blade Glide (KDB Glide) is a medical device that received FDA 510(k) clearance on 2024-05-17. The listed applicant is New World Medical, Inc.. The 510(k) number is K220891.
When did Kahook Dual Blade Glide (KDB Glide) receive FDA 510(k) clearance?
Kahook Dual Blade Glide (KDB Glide) received FDA 510(k) clearance on 2024-05-17, under 510(k) number K220891.
Who is the listed applicant for Kahook Dual Blade Glide (KDB Glide)?
The FDA 510(k) record lists New World Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Kahook Dual Blade Glide (KDB Glide)?
The FDA product code for Kahook Dual Blade Glide (KDB Glide) is QUQ.
相关临床试验
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列明New World Medical, 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。
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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