KeyPrint KeySplint Hard
K号: K203000 · 2021-04-09
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器械摘要
KeyPrint KeySplint Hard is the device name listed in this FDA 510(k) record. The listed applicant is Mycone Dental Supply Co. Inc. (Dba Keystone Industries). It received FDA 510(k) clearance on 2021-04-09 under 510(k) number K203000. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.
常见问题
What is the KeyPrint KeySplint Hard?
KeyPrint KeySplint Hard is a medical device that received FDA 510(k) clearance on 2021-04-09. The listed applicant is Mycone Dental Supply Co. Inc. (Dba Keystone Industries). The 510(k) number is K203000.
When did KeyPrint KeySplint Hard receive FDA 510(k) clearance?
KeyPrint KeySplint Hard received FDA 510(k) clearance on 2021-04-09, under 510(k) number K203000.
Who is the listed applicant for KeyPrint KeySplint Hard?
The FDA 510(k) record lists Mycone Dental Supply Co. Inc. (Dba Keystone Industries) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KeyPrint KeySplint Hard?
The FDA product code for KeyPrint KeySplint Hard is MQC.
相关临床试验
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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