InVivo 网络查看器
K号: K181926 · 2018-09-21
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器械摘要
InVivo Web Viewer is the device name listed in this FDA 510(k) record. The listed applicant is Anatomage, Inc.. It received FDA 510(k) clearance on 2018-09-21 under 510(k) number K181926. 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 InVivo Web Viewer?
InVivo Web Viewer is a medical device that received FDA 510(k) clearance on 2018-09-21. The listed applicant is Anatomage, Inc.. The 510(k) number is K181926.
When did InVivo Web Viewer receive FDA 510(k) clearance?
InVivo Web Viewer received FDA 510(k) clearance on 2018-09-21, under 510(k) number K181926.
Who is the listed applicant for InVivo Web Viewer?
The FDA 510(k) record lists Anatomage, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for InVivo Web Viewer?
The FDA product code for InVivo Web Viewer is LLZ.
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列明Anatomage, Inc.为申报人的其他记录
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相关器械（代码：LLZ）
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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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