COMPACT S，COMPACT S (LED)
K号: K170104 · 2017-12-27
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决定日期2017-12-27
产品代码ELC
咨询委员会DE
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决定实质等同
器械摘要
COMPACT S, COMPACT S (LED) is the device name listed in this FDA 510(k) record. The listed applicant is Dmetec.Co., Ltd.. It received FDA 510(k) clearance on 2017-12-27 under 510(k) number K170104. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the COMPACT S, COMPACT S (LED)?
COMPACT S, COMPACT S (LED) is a medical device that received FDA 510(k) clearance on 2017-12-27. The listed applicant is Dmetec.Co., Ltd.. The 510(k) number is K170104.
When did COMPACT S, COMPACT S (LED) receive FDA 510(k) clearance?
COMPACT S, COMPACT S (LED) received FDA 510(k) clearance on 2017-12-27, under 510(k) number K170104.
Who is the listed applicant for COMPACT S, COMPACT S (LED)?
The FDA 510(k) record lists Dmetec.Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COMPACT S, COMPACT S (LED)?
The FDA product code for COMPACT S, COMPACT S (LED) is ELC.
相关临床试验
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相关器械（代码：ELC）
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。
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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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