Liposaver
K号: K212969 · 2024-08-07
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决定日期2024-08-07
产品代码QPB
咨询委员会SU
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决定实质等同
器械摘要
Liposaver is the device name listed in this FDA 510(k) record. The listed applicant is Lhbiomed Co., Ltd.. It received FDA 510(k) clearance on 2024-08-07 under 510(k) number K212969. The device is classified under product code QPB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Liposaver?
Liposaver is a medical device that received FDA 510(k) clearance on 2024-08-07. The listed applicant is Lhbiomed Co., Ltd.. The 510(k) number is K212969.
When did Liposaver receive FDA 510(k) clearance?
Liposaver received FDA 510(k) clearance on 2024-08-07, under 510(k) number K212969.
Who is the listed applicant for Liposaver?
The FDA 510(k) record lists Lhbiomed Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Liposaver?
The FDA product code for Liposaver is QPB.
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：QPB）
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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