Myomics Q
K号: K211432 · 2021-11-23
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器械摘要
Myomics Q is the device name listed in this FDA 510(k) record. The listed applicant is Phantomics, Inc.. It received FDA 510(k) clearance on 2021-11-23 under 510(k) number K211432. 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 Myomics Q?
Myomics Q is a medical device that received FDA 510(k) clearance on 2021-11-23. The listed applicant is Phantomics, Inc.. The 510(k) number is K211432.
When did Myomics Q receive FDA 510(k) clearance?
Myomics Q received FDA 510(k) clearance on 2021-11-23, under 510(k) number K211432.
Who is the listed applicant for Myomics Q?
The FDA 510(k) record lists Phantomics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Myomics Q?
The FDA product code for Myomics Q is LLZ.
相关临床试验
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列明Phantomics, 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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