Leica FL560
K号: K170239 · 2017-07-05
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器械摘要
Leica FL560 is the device name listed in this FDA 510(k) record. The listed applicant is Leica Microsystems (Schweiz) AG. It received FDA 510(k) clearance on 2017-07-05 under 510(k) number K170239. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Unknown.
常见问题
What is the Leica FL560?
Leica FL560 is a medical device that received FDA 510(k) clearance on 2017-07-05. The listed applicant is Leica Microsystems (Schweiz) AG. The 510(k) number is K170239.
When did Leica FL560 receive FDA 510(k) clearance?
Leica FL560 received FDA 510(k) clearance on 2017-07-05, under 510(k) number K170239.
Who is the listed applicant for Leica FL560?
The FDA 510(k) record lists Leica Microsystems (Schweiz) AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Leica FL560?
The FDA product code for Leica FL560 is IZI.
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Leica Microsystems (Schweiz) AG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：IZI）
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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