SimpleSense-BP,SimpleSense-BP 软件应用
K号: K232053 · 2023-12-08
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器械摘要
常见问题
What is the SimpleSense-BP, SimpleSense-BP Software Application?
SimpleSense-BP, SimpleSense-BP Software Application is a medical device that received FDA 510(k) clearance on 2023-12-08. The listed applicant is Nanowear, Inc.. The 510(k) number is K232053.
When did SimpleSense-BP, SimpleSense-BP Software Application receive FDA 510(k) clearance?
SimpleSense-BP, SimpleSense-BP Software Application received FDA 510(k) clearance on 2023-12-08, under 510(k) number K232053.
Who is the listed applicant for SimpleSense-BP, SimpleSense-BP Software Application?
The FDA 510(k) record lists Nanowear, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SimpleSense-BP, SimpleSense-BP Software Application?
The FDA product code for SimpleSense-BP, SimpleSense-BP Software Application 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Nanowear, 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: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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