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FDA 510(k)

MICOR 镜片破碎系统

K号: K214028 · 2022-09-09

决定日期2022-09-09
产品代码HQC
咨询委员会OP 请注意,由于您没有提供具体的医疗设备监管文本,我无法进行翻译。请提供具体的文本内容,以便我能够按照您的要求进行翻译。
决定实质等同

器械摘要

MICOR Lens Fragmentation System 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 2022-09-09 under 510(k) number K214028. 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 Lens Fragmentation System?

MICOR Lens Fragmentation System is a medical device that received FDA 510(k) clearance on 2022-09-09. The listed applicant is Carl Zeiss Meditec Cataract Technology, Inc.. The 510(k) number is K214028.

When did MICOR Lens Fragmentation System receive FDA 510(k) clearance?

MICOR Lens Fragmentation System received FDA 510(k) clearance on 2022-09-09, under 510(k) number K214028.

Who is the listed applicant for MICOR Lens Fragmentation System?

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 Lens Fragmentation System?

The FDA product code for MICOR Lens Fragmentation System is HQC.

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列明Carl Zeiss Meditec Cataract Technology, Inc.为申报人的其他记录

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相关器械(代码:HQC)

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官方来源

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