ImaCor Zura手持式ZHH-010
K号: K220490 · 2022-04-08
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器械摘要
ImaCor Zura Handheld ZHH-010 is the device name listed in this FDA 510(k) record. The listed applicant is Imacor, Inc.. It received FDA 510(k) clearance on 2022-04-08 under 510(k) number K220490. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the ImaCor Zura Handheld ZHH-010?
ImaCor Zura Handheld ZHH-010 is a medical device that received FDA 510(k) clearance on 2022-04-08. The listed applicant is Imacor, Inc.. The 510(k) number is K220490.
When did ImaCor Zura Handheld ZHH-010 receive FDA 510(k) clearance?
ImaCor Zura Handheld ZHH-010 received FDA 510(k) clearance on 2022-04-08, under 510(k) number K220490.
Who is the listed applicant for ImaCor Zura Handheld ZHH-010?
The FDA 510(k) record lists Imacor, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ImaCor Zura Handheld ZHH-010?
The FDA product code for ImaCor Zura Handheld ZHH-010 is IYN.
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相关器械（代码：IYN）
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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