InBody 血压计,型号 BPBIO480KV
K号: K221764 · 2022-10-07
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器械摘要
常见问题
What is the InBody Blood pressure monitor, Model BPBIO480KV?
InBody Blood pressure monitor, Model BPBIO480KV is a medical device that received FDA 510(k) clearance on 2022-10-07. The listed applicant is Inbody Co., Ltd.. The 510(k) number is K221764.
When did InBody Blood pressure monitor, Model BPBIO480KV receive FDA 510(k) clearance?
InBody Blood pressure monitor, Model BPBIO480KV received FDA 510(k) clearance on 2022-10-07, under 510(k) number K221764.
Who is the listed applicant for InBody Blood pressure monitor, Model BPBIO480KV?
The FDA 510(k) record lists Inbody Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for InBody Blood pressure monitor, Model BPBIO480KV?
The FDA product code for InBody Blood pressure monitor, Model BPBIO480KV is DXN.
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。
列明Inbody Co., Ltd.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:DXN)
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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