Jac-Cell 医疗测试仪
K号: K170105 · 2017-02-28
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器械摘要
Jac-Cell Medic testers is the device name listed in this FDA 510(k) record. The listed applicant is Jac-Cell Medic. It received FDA 510(k) clearance on 2017-02-28 under 510(k) number K170105. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Jac-Cell Medic testers?
Jac-Cell Medic testers is a medical device that received FDA 510(k) clearance on 2017-02-28. The listed applicant is Jac-Cell Medic. The 510(k) number is K170105.
When did Jac-Cell Medic testers receive FDA 510(k) clearance?
Jac-Cell Medic testers received FDA 510(k) clearance on 2017-02-28, under 510(k) number K170105.
Who is the listed applicant for Jac-Cell Medic testers?
The FDA 510(k) record lists Jac-Cell Medic as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Jac-Cell Medic testers?
The FDA product code for Jac-Cell Medic testers is GEI.
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：GEI）
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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