Image Management V15
K号: K240822 · 2024-04-24
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器械摘要
Image Management V15 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems Technologies. It received FDA 510(k) clearance on 2024-04-24 under 510(k) number K240822. 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 Image Management V15?
Image Management V15 is a medical device that received FDA 510(k) clearance on 2024-04-24. The listed applicant is Philips Medical Systems Technologies. The 510(k) number is K240822.
When did Image Management V15 receive FDA 510(k) clearance?
Image Management V15 received FDA 510(k) clearance on 2024-04-24, under 510(k) number K240822.
Who is the listed applicant for Image Management V15?
The FDA 510(k) record lists Philips Medical Systems Technologies as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Image Management V15?
The FDA product code for Image Management V15 is LLZ.
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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。
K261874Syneris PACS v.1.0.1.0SynerisK262442HipStudio分析Replasia BVK261855Elucid PlaqueIQElucid Bioimaging, Inc.K254214OOOPDS
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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