BSD3543W
K号: K200787 · 2020-04-23
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器械摘要
BSD3543W is the device name listed in this FDA 510(k) record. The listed applicant is Bontech Co., Ltd.. It received FDA 510(k) clearance on 2020-04-23 under 510(k) number K200787. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the BSD3543W?
BSD3543W is a medical device that received FDA 510(k) clearance on 2020-04-23. The listed applicant is Bontech Co., Ltd.. The 510(k) number is K200787.
When did BSD3543W receive FDA 510(k) clearance?
BSD3543W received FDA 510(k) clearance on 2020-04-23, under 510(k) number K200787.
Who is the listed applicant for BSD3543W?
The FDA 510(k) record lists Bontech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BSD3543W?
The FDA product code for BSD3543W is MQB.
列明Bontech 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：MQB）
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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