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FDA 510(k)

MEDRAD 成像大批量包装转移针头

K号: K200280 · 2020-07-30

决定日期2020-07-30
产品代码PQH
咨询委员会医疗设备监管文本翻译如下: HO 请注意,由于您没有提供具体的医疗设备监管文本内容,以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
决定实质等同

器械摘要

MEDRAD Imaging Bulk Package Transfer Spike is the device name listed in this FDA 510(k) record. The listed applicant is Bayer Medical Care, Inc.. It received FDA 510(k) clearance on 2020-07-30 under 510(k) number K200280. The device is classified under product code PQH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the MEDRAD Imaging Bulk Package Transfer Spike?

MEDRAD Imaging Bulk Package Transfer Spike is a medical device that received FDA 510(k) clearance on 2020-07-30. The listed applicant is Bayer Medical Care, Inc.. The 510(k) number is K200280.

When did MEDRAD Imaging Bulk Package Transfer Spike receive FDA 510(k) clearance?

MEDRAD Imaging Bulk Package Transfer Spike received FDA 510(k) clearance on 2020-07-30, under 510(k) number K200280.

Who is the listed applicant for MEDRAD Imaging Bulk Package Transfer Spike?

The FDA 510(k) record lists Bayer Medical Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDRAD Imaging Bulk Package Transfer Spike?

The FDA product code for MEDRAD Imaging Bulk Package Transfer Spike is PQH.

相关临床试验

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列明Bayer Medical Care, Inc.为申报人的其他记录

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相关器械(代码:PQH)

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。

官方来源

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