Spo2传感器
K号: K202851 · 2020-11-27
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申请人Jkh USA, LLC
决定日期2020-11-27
产品代码DQA
咨询委员会CV
请注意，由于原文未提供具体内容，以下是一个示例翻译：
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产品名称：[产品名称]
公司名称：[公司名称]
FDA批准号：[FDA批准号]
510(k)申请号：[510(k)申请号]
PMA申请号：[PMA申请号]
临床试验注册号：[NCT]
PubMed ID：[PMID]
产品标识符：[标识符]
产品URL：[URL]
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请将上述示例中的[产品名称]、[公司名称]、[FDA批准号]等占位符替换为实际内容。
决定实质等同
器械摘要
Spo2 Sensor is the device name listed in this FDA 510(k) record. The listed applicant is Jkh USA, LLC. It received FDA 510(k) clearance on 2020-11-27 under 510(k) number K202851. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Spo2 Sensor?
Spo2 Sensor is a medical device that received FDA 510(k) clearance on 2020-11-27. The listed applicant is Jkh USA, LLC. The 510(k) number is K202851.
When did Spo2 Sensor receive FDA 510(k) clearance?
Spo2 Sensor received FDA 510(k) clearance on 2020-11-27, under 510(k) number K202851.
Who is the listed applicant for Spo2 Sensor?
The FDA 510(k) record lists Jkh USA, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Spo2 Sensor?
The FDA product code for Spo2 Sensor is DQA.
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。
列明Jkh USA, LLC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。
K203636PlusCare 温度探头，皮肤类型：PT2252-AS，PTHP-AS，PTMQ-AS，PTSW-AS，PTSM-15AS，PTSL-AS，PTMR-AS；直肠类型：PT2252-AG，PTHP-AG，PTMQ-AG，PTSW-AG，PTSM-15AG，PTSL-AG，PTMR-AGK203635患者监护电缆K203652血压计，U1883S,U1883D, U1882S, U1882D, U1881S, U1881D, 血压计，U1885S, U1885D, U1880S, U1880D, U1886S, U1886D, 血压计，U1869S, U1869D, U1889S, U1889D, U1884S, U1884D, 血压计，U1710S, U1720S, U1730S,U1740S, U1750S, U1760S, 血压计，U1770S, U1790s, U1710D, U1720D, U1730D, U1740DK201645按摩压缩靴K201470一次性医用口罩K182671Medi-Direct TENS 笔
相关器械（代码：DQA）
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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