iQMR
K号: K173605 · 2018-03-08
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器械摘要
iQMR is the device name listed in this FDA 510(k) record. The listed applicant is Medic Vision - Imaging Solutions, Ltd.. It received FDA 510(k) clearance on 2018-03-08 under 510(k) number K173605. 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 iQMR?
iQMR is a medical device that received FDA 510(k) clearance on 2018-03-08. The listed applicant is Medic Vision - Imaging Solutions, Ltd.. The 510(k) number is K173605.
When did iQMR receive FDA 510(k) clearance?
iQMR received FDA 510(k) clearance on 2018-03-08, under 510(k) number K173605.
Who is the listed applicant for iQMR?
The FDA 510(k) record lists Medic Vision - Imaging Solutions, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for iQMR?
The FDA product code for iQMR is LLZ.
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
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