Philips CombiDiagnost R90
K号: K163210 · 2017-01-31
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器械摘要
Philips CombiDiagnost R90 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems Dmc GmbH. It received FDA 510(k) clearance on 2017-01-31 under 510(k) number K163210. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Philips CombiDiagnost R90?
Philips CombiDiagnost R90 is a medical device that received FDA 510(k) clearance on 2017-01-31. The listed applicant is Philips Medical Systems Dmc GmbH. The 510(k) number is K163210.
When did Philips CombiDiagnost R90 receive FDA 510(k) clearance?
Philips CombiDiagnost R90 received FDA 510(k) clearance on 2017-01-31, under 510(k) number K163210.
Who is the listed applicant for Philips CombiDiagnost R90?
The FDA 510(k) record lists Philips Medical Systems Dmc GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Philips CombiDiagnost R90?
The FDA product code for Philips CombiDiagnost R90 is JAA.
相关临床试验
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列明Philips Medical Systems Dmc GmbH为申报人的其他记录
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。
相关器械（代码：JAA）
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。
K253103Nexus DRF 数字X射线成像系统Varex Imaging CorporationK251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLCK242488Soteria E-ViewOmega Medical Imaging, LLCK242948Adora DRFi (04550010)Nrt X-Ray A/SK233380TRIDENT 移动荧光透视系统Dornier Medtech AmericaK233945ProxiDiagnost N90 / Precision CRF (706110, 706400)Philips Medical Systems Dmc GmbH
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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