FROG 力钳阀 (VAL1-F1-100)
K号: K221264 · 2022-06-01
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决定日期2022-06-01
产品代码ODC
咨询委员会GU
请注意，由于您只提供了“GU”这个词，我无法提供完整的翻译。如果您能提供完整的句子或段落，我将能够为您提供准确的翻译。
决定实质等同
器械摘要
FROG Forceps Valve (VAL1-F1-100) is the device name listed in this FDA 510(k) record. The listed applicant is Fujifilm Medwork GmbH. It received FDA 510(k) clearance on 2022-06-01 under 510(k) number K221264. The device is classified under product code ODC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the FROG Forceps Valve (VAL1-F1-100)?
FROG Forceps Valve (VAL1-F1-100) is a medical device that received FDA 510(k) clearance on 2022-06-01. The listed applicant is Fujifilm Medwork GmbH. The 510(k) number is K221264.
When did FROG Forceps Valve (VAL1-F1-100) receive FDA 510(k) clearance?
FROG Forceps Valve (VAL1-F1-100) received FDA 510(k) clearance on 2022-06-01, under 510(k) number K221264.
Who is the listed applicant for FROG Forceps Valve (VAL1-F1-100)?
The FDA 510(k) record lists Fujifilm Medwork GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FROG Forceps Valve (VAL1-F1-100)?
The FDA product code for FROG Forceps Valve (VAL1-F1-100) is ODC.
相关临床试验
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列明Fujifilm Medwork GmbH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：ODC）
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
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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