Choice 2 DC
K号: K250156 · 2025-07-11
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申请人Bisco, Inc.
决定日期2025-07-11
产品代码EMA
咨询委员会DE
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决定实质等同
器械摘要
Choice 2 DC is the device name listed in this FDA 510(k) record. The listed applicant is Bisco, Inc.. It received FDA 510(k) clearance on 2025-07-11 under 510(k) number K250156. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Choice 2 DC?
Choice 2 DC is a medical device that received FDA 510(k) clearance on 2025-07-11. The listed applicant is Bisco, Inc.. The 510(k) number is K250156.
When did Choice 2 DC receive FDA 510(k) clearance?
Choice 2 DC received FDA 510(k) clearance on 2025-07-11, under 510(k) number K250156.
Who is the listed applicant for Choice 2 DC?
The FDA 510(k) record lists Bisco, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Choice 2 DC?
The FDA product code for Choice 2 DC is EMA.
相关临床试验
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列明Bisco, Inc.为申报人的其他记录
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相关器械（代码：EMA）
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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