KeyPrint KeySplint Soft
K号: K183598 · 2019-11-15
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器械摘要
KeyPrint KeySplint Soft is the device name listed in this FDA 510(k) record. The listed applicant is Keystone Industries. It received FDA 510(k) clearance on 2019-11-15 under 510(k) number K183598. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.
常见问题
What is the KeyPrint KeySplint Soft?
KeyPrint KeySplint Soft is a medical device that received FDA 510(k) clearance on 2019-11-15. The listed applicant is Keystone Industries. The 510(k) number is K183598.
When did KeyPrint KeySplint Soft receive FDA 510(k) clearance?
KeyPrint KeySplint Soft received FDA 510(k) clearance on 2019-11-15, under 510(k) number K183598.
Who is the listed applicant for KeyPrint KeySplint Soft?
The FDA 510(k) record lists Keystone Industries as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KeyPrint KeySplint Soft?
The FDA product code for KeyPrint KeySplint Soft is MQC.
相关临床试验
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列明Keystone Industries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：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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