安在 呼吸门控系统
K号: K170719 · 2017-04-05
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器械摘要
Anzai Respiratory Gating System is the device name listed in this FDA 510(k) record. The listed applicant is Anzai Medical Co., Ltd.. It received FDA 510(k) clearance on 2017-04-05 under 510(k) number K170719. The device is classified under product code LHN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Anzai Respiratory Gating System?
Anzai Respiratory Gating System is a medical device that received FDA 510(k) clearance on 2017-04-05. The listed applicant is Anzai Medical Co., Ltd.. The 510(k) number is K170719.
When did Anzai Respiratory Gating System receive FDA 510(k) clearance?
Anzai Respiratory Gating System received FDA 510(k) clearance on 2017-04-05, under 510(k) number K170719.
Who is the listed applicant for Anzai Respiratory Gating System?
The FDA 510(k) record lists Anzai Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Anzai Respiratory Gating System?
The FDA product code for Anzai Respiratory Gating System is LHN.
相关临床试验
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列明Anzai Medical Co., Ltd.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：LHN）
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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