FDA 510(k)MICOR 700 自动 I/A
K号: K243395 · 2025-08-08
决定日期2025-08-08
产品代码HQC
咨询委员会OP
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决定实质等同
器械摘要
MICOR 700 with Auto I/A is the device name listed in this FDA 510(k) record. The listed applicant is Carl Zeiss Meditec Cataract Technology, Inc.. It received FDA 510(k) clearance on 2025-08-08 under 510(k) number K243395. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MICOR 700 with Auto I/A?
MICOR 700 with Auto I/A is a medical device that received FDA 510(k) clearance on 2025-08-08. The listed applicant is Carl Zeiss Meditec Cataract Technology, Inc.. The 510(k) number is K243395.
When did MICOR 700 with Auto I/A receive FDA 510(k) clearance?
MICOR 700 with Auto I/A received FDA 510(k) clearance on 2025-08-08, under 510(k) number K243395.
Who is the listed applicant for MICOR 700 with Auto I/A?
The FDA 510(k) record lists Carl Zeiss Meditec Cataract Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICOR 700 with Auto I/A?
The FDA product code for MICOR 700 with Auto I/A is HQC.
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列明Carl Zeiss Meditec Cataract Technology, Inc.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。
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相关器械(代码:HQC)
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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