Restore PACS
K号: K162141 · 2016-09-02
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器械摘要
Restore PACS is the device name listed in this FDA 510(k) record. The listed applicant is Xian Wingspan Electronic Technology Co., Ltd.. It received FDA 510(k) clearance on 2016-09-02 under 510(k) number K162141. 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 Restore PACS?
Restore PACS is a medical device that received FDA 510(k) clearance on 2016-09-02. The listed applicant is Xian Wingspan Electronic Technology Co., Ltd.. The 510(k) number is K162141.
When did Restore PACS receive FDA 510(k) clearance?
Restore PACS received FDA 510(k) clearance on 2016-09-02, under 510(k) number K162141.
Who is the listed applicant for Restore PACS?
The FDA 510(k) record lists Xian Wingspan Electronic Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Restore PACS?
The FDA product code for Restore PACS is LLZ.
相关临床试验
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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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