TRIDENT 移动荧光透视系统
K号: K233380 · 2024-06-26
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器械摘要
TRIDENT Mobile Fluoroscopy System is the device name listed in this FDA 510(k) record. The listed applicant is Dornier Medtech America. It received FDA 510(k) clearance on 2024-06-26 under 510(k) number K233380. 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 TRIDENT Mobile Fluoroscopy System?
TRIDENT Mobile Fluoroscopy System is a medical device that received FDA 510(k) clearance on 2024-06-26. The listed applicant is Dornier Medtech America. The 510(k) number is K233380.
When did TRIDENT Mobile Fluoroscopy System receive FDA 510(k) clearance?
TRIDENT Mobile Fluoroscopy System received FDA 510(k) clearance on 2024-06-26, under 510(k) number K233380.
Who is the listed applicant for TRIDENT Mobile Fluoroscopy System?
The FDA 510(k) record lists Dornier Medtech America as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRIDENT Mobile Fluoroscopy System?
The FDA product code for TRIDENT Mobile Fluoroscopy System is JAA.
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列明Dornier Medtech America为申报人的其他记录
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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/SK233945ProxiDiagnost N90 / Precision CRF (706110, 706400)Philips Medical Systems Dmc GmbHK232910CombiDiagnost R90Philips 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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