Greenmedi Safety Filter Syringe
K号: K173743 · 2019-01-28
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决定日期2019-01-28
产品代码MEG
咨询委员会医疗设备监管文本翻译如下：
HO
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决定实质等同
器械摘要
Greenmedi Safety Filter Syringe is the device name listed in this FDA 510(k) record. The listed applicant is Sang-A Frontec Co., Ltd.. It received FDA 510(k) clearance on 2019-01-28 under 510(k) number K173743. The device is classified under product code MEG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Greenmedi Safety Filter Syringe?
Greenmedi Safety Filter Syringe is a medical device that received FDA 510(k) clearance on 2019-01-28. The listed applicant is Sang-A Frontec Co., Ltd.. The 510(k) number is K173743.
When did Greenmedi Safety Filter Syringe receive FDA 510(k) clearance?
Greenmedi Safety Filter Syringe received FDA 510(k) clearance on 2019-01-28, under 510(k) number K173743.
Who is the listed applicant for Greenmedi Safety Filter Syringe?
The FDA 510(k) record lists Sang-A Frontec Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Greenmedi Safety Filter Syringe?
The FDA product code for Greenmedi Safety Filter Syringe is MEG.
相关临床试验
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相关器械（代码：MEG）
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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