Cryotec
K号: K162051 · 2016-12-14
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决定日期2016-12-14
产品代码MQK
咨询委员会OB
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决定实质等同
器械摘要
Cryotec is the device name listed in this FDA 510(k) record. The listed applicant is Reprolife, Inc.. It received FDA 510(k) clearance on 2016-12-14 under 510(k) number K162051. The device is classified under product code MQK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Cryotec?
Cryotec is a medical device that received FDA 510(k) clearance on 2016-12-14. The listed applicant is Reprolife, Inc.. The 510(k) number is K162051.
When did Cryotec receive FDA 510(k) clearance?
Cryotec received FDA 510(k) clearance on 2016-12-14, under 510(k) number K162051.
Who is the listed applicant for Cryotec?
The FDA 510(k) record lists Reprolife, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cryotec?
The FDA product code for Cryotec is MQK.
相关临床试验
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相关器械（代码：MQK）
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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