Bel-Cypher Pro
K号: K163175 · 2017-03-20
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决定日期2017-03-20
产品代码MUH
咨询委员会DE
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器械摘要
Bel-Cypher Pro is the device name listed in this FDA 510(k) record. The listed applicant is Takara Belmont Corporation. It received FDA 510(k) clearance on 2017-03-20 under 510(k) number K163175. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Bel-Cypher Pro?
Bel-Cypher Pro is a medical device that received FDA 510(k) clearance on 2017-03-20. The listed applicant is Takara Belmont Corporation. The 510(k) number is K163175.
When did Bel-Cypher Pro receive FDA 510(k) clearance?
Bel-Cypher Pro received FDA 510(k) clearance on 2017-03-20, under 510(k) number K163175.
Who is the listed applicant for Bel-Cypher Pro?
The FDA 510(k) record lists Takara Belmont Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Bel-Cypher Pro?
The FDA product code for Bel-Cypher Pro is MUH.
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Takara Belmont Corporation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：MUH）
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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