Konicaminolta DI-X1
K号: K182431 · 2018-11-26
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器械摘要
Konicaminolta DI-X1 is the device name listed in this FDA 510(k) record. The listed applicant is Konica Minolta, Inc.. It received FDA 510(k) clearance on 2018-11-26 under 510(k) number K182431. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Konicaminolta DI-X1?
Konicaminolta DI-X1 is a medical device that received FDA 510(k) clearance on 2018-11-26. The listed applicant is Konica Minolta, Inc.. The 510(k) number is K182431.
When did Konicaminolta DI-X1 receive FDA 510(k) clearance?
Konicaminolta DI-X1 received FDA 510(k) clearance on 2018-11-26, under 510(k) number K182431.
Who is the listed applicant for Konicaminolta DI-X1?
The FDA 510(k) record lists Konica Minolta, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Konicaminolta DI-X1?
The FDA product code for Konicaminolta DI-X1 is LLZ.
相关临床试验
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列明Konica Minolta, Inc.为申报人的其他记录
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相关器械（代码：LLZ）
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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请注意，由于您没有提供具体的医疗设备监管文本，我无法提供准确的翻译。如果您能提供具体的文本内容，我将能够为您提供准确的翻译。Taiwan Main Orthopaedic Biotechnology Co., Ltd.K261861SPINEsim v1.0Mdsim S.A.K2620603D-RD-SRadiopharmaceutical Imaging & Dosimetry, LLC
官方来源
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