VITEK 2 AST-酵母 阿尼鲁兰(<= 0.015 - >= 8 µg/mL)
K号: K232963 · 2024-06-07
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器械摘要
常见问题
What is the VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL)?
VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL) is a medical device that received FDA 510(k) clearance on 2024-06-07. The listed applicant is bioMerieux, Inc.. The 510(k) number is K232963.
When did VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL) receive FDA 510(k) clearance?
VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL) received FDA 510(k) clearance on 2024-06-07, under 510(k) number K232963.
Who is the listed applicant for VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL)?
The FDA 510(k) record lists bioMerieux, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL)?
The FDA product code for VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL) is NGZ.
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bioMerieux, 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:NGZ)
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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