GR 树脂系统 MSI
K号: K231775 · 2024-08-08
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器械摘要
GR Resin System MSI is the device name listed in this FDA 510(k) record. The listed applicant is Pro3Dure Medical. It received FDA 510(k) clearance on 2024-08-08 under 510(k) number K231775. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.
常见问题
What is the GR Resin System MSI?
GR Resin System MSI is a medical device that received FDA 510(k) clearance on 2024-08-08. The listed applicant is Pro3Dure Medical. The 510(k) number is K231775.
When did GR Resin System MSI receive FDA 510(k) clearance?
GR Resin System MSI received FDA 510(k) clearance on 2024-08-08, under 510(k) number K231775.
Who is the listed applicant for GR Resin System MSI?
The FDA 510(k) record lists Pro3Dure Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GR Resin System MSI?
The FDA product code for GR Resin System MSI is MQC.
相关临床试验
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相关器械（代码：MQC）
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。
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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