Insight BD
K号: K172832 · 2018-02-06
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器械摘要
Insight BD is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medi Cal Solutions, Inc.. It received FDA 510(k) clearance on 2018-02-06 under 510(k) number K172832. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Insight BD?
Insight BD is a medical device that received FDA 510(k) clearance on 2018-02-06. The listed applicant is Siemens Medi Cal Solutions, Inc.. The 510(k) number is K172832.
When did Insight BD receive FDA 510(k) clearance?
Insight BD received FDA 510(k) clearance on 2018-02-06, under 510(k) number K172832.
Who is the listed applicant for Insight BD?
The FDA 510(k) record lists Siemens Medi Cal Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Insight BD?
The FDA product code for Insight BD is LLZ.
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列明Siemens Medi Cal Solutions, Inc.为申报人的其他记录
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相关器械（代码：LLZ）
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
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