CORIOGRAPH 术前规划和建模服务
K号: K242272 · 2024-11-15
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器械摘要
CORIOGRAPH Pre-Op Planning and Modeling Services is the device name listed in this FDA 510(k) record. The listed applicant is Blue Belt Technologies, Inc.. It received FDA 510(k) clearance on 2024-11-15 under 510(k) number K242272. FDA Decision: Substantially Equivalent.
常见问题
What is the CORIOGRAPH Pre-Op Planning and Modeling Services?
CORIOGRAPH Pre-Op Planning and Modeling Services is a medical device that received FDA 510(k) clearance on 2024-11-15. The listed applicant is Blue Belt Technologies, Inc.. The 510(k) number is K242272.
When did CORIOGRAPH Pre-Op Planning and Modeling Services receive FDA 510(k) clearance?
CORIOGRAPH Pre-Op Planning and Modeling Services received FDA 510(k) clearance on 2024-11-15, under 510(k) number K242272.
Who is the listed applicant for CORIOGRAPH Pre-Op Planning and Modeling Services?
The FDA 510(k) record lists Blue Belt Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
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Blue Belt Technologies, 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。
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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