Carescape SpO2 - Masimo
K号: K212876 · 2021-10-08
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决定日期2021-10-08
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
Carescape SpO2 - Masimo is the device name listed in this FDA 510(k) record. The listed applicant is Masimo Corporation. It received FDA 510(k) clearance on 2021-10-08 under 510(k) number K212876. 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 Carescape SpO2 - Masimo?
Carescape SpO2 - Masimo is a medical device that received FDA 510(k) clearance on 2021-10-08. The listed applicant is Masimo Corporation. The 510(k) number is K212876.
When did Carescape SpO2 - Masimo receive FDA 510(k) clearance?
Carescape SpO2 - Masimo received FDA 510(k) clearance on 2021-10-08, under 510(k) number K212876.
Who is the listed applicant for Carescape SpO2 - Masimo?
FDA 510(k)记录显示Masimo公司为申请人。这本身并不能确立该设备制造商的身份。
What is the FDA product code for Carescape SpO2 - Masimo?
The FDA product code for Carescape SpO2 - Masimo 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Masimo Corporation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: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。
K252821可重复使用成人SpO2夹式传感器(3m)(M1196A);可重复使用成人SpO2夹式传感器(0.9m)(M1196T)Philips Medizin Systeme Böblingen GmbHK252655脉搏血氧仪(PO-A2AO,PO-A2AT,PO-A3AO,PO-H1AO,PO-B1AO,PO-C5AO,PO-C5AT,PO-C6AO, PO-C6AT)Shenzhen Imdk Medical Technology Co., Ltd.K253887鼻翼SpO2传感器(989803205381);鼻翼SpO2传感器(989803205391);鼻翼Sp02传感器(989803205401)Philips Medizin SystemeK260931Unimed可重复使用指夹式SpO2传感器(U403-49R和U103-49R)Unimed Medical Supplies, Inc.K252448AViTA 脉搏血氧仪 (SP61)Avita CorporationK252805优威尔®指夹式脉搏血氧仪(YX105,YX106,YX110,YX310)Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.
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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