CryoIQ DERM,CryoIQ PRO,CryoIQ EquiMED
K号: K172049 · 2017-08-30
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器械摘要
常见问题
What is the CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED?
CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED is a medical device that received FDA 510(k) clearance on 2017-08-30. The listed applicant is Cry IQ AB. The 510(k) number is K172049.
When did CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED receive FDA 510(k) clearance?
CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED received FDA 510(k) clearance on 2017-08-30, under 510(k) number K172049.
Who is the listed applicant for CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED?
The FDA 510(k) record lists Cry IQ AB as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED?
The FDA product code for CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED is GEH.
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。
相关器械(代码:GEH)
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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