Ez3D-i/E3
K号: K222069 · 2022-09-06
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器械摘要
Ez3D-i/E3 is the device name listed in this FDA 510(k) record. The listed applicant is Ewoosoft Co., Ltd.. It received FDA 510(k) clearance on 2022-09-06 under 510(k) number K222069. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Ez3D-i/E3?
Ez3D-i/E3 is a medical device that received FDA 510(k) clearance on 2022-09-06. The listed applicant is Ewoosoft Co., Ltd.. The 510(k) number is K222069.
When did Ez3D-i/E3 receive FDA 510(k) clearance?
Ez3D-i/E3 received FDA 510(k) clearance on 2022-09-06, under 510(k) number K222069.
Who is the listed applicant for Ez3D-i/E3?
The FDA 510(k) record lists Ewoosoft Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ez3D-i/E3?
The FDA product code for Ez3D-i/E3 is LLZ.
列明Ewoosoft 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：LLZ）
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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