MEDO-甲状腺
K号: K203502 · 2021-04-23
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器械摘要
MEDO-Thyroid is the device name listed in this FDA 510(k) record. The listed applicant is Medo DX Pte. , Ltd.. It received FDA 510(k) clearance on 2021-04-23 under 510(k) number K203502. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MEDO-Thyroid?
MEDO-Thyroid is a medical device that received FDA 510(k) clearance on 2021-04-23. The listed applicant is Medo DX Pte. , Ltd.. The 510(k) number is K203502.
When did MEDO-Thyroid receive FDA 510(k) clearance?
MEDO-Thyroid received FDA 510(k) clearance on 2021-04-23, under 510(k) number K203502.
Who is the listed applicant for MEDO-Thyroid?
The FDA 510(k) record lists Medo DX Pte. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDO-Thyroid?
The FDA product code for MEDO-Thyroid is QIH.
相关临床试验
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相关器械（代码：QIH）
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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