FDA 510(k)

Finger Pulse Oximeter, Model: X1906P

K号: K221798 · 2023-05-04

申请人Shenzhen Changkun Technology Co., Ltd.

决定日期2023-05-04

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： --- 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] --- 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

Finger Pulse Oximeter, Model: X1906P is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Changkun Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-05-04 under 510(k) number K221798. 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 Finger Pulse Oximeter, Model: X1906P?

Finger Pulse Oximeter, Model: X1906P is a medical device that received FDA 510(k) clearance on 2023-05-04. The listed applicant is Shenzhen Changkun Technology Co., Ltd.. The 510(k) number is K221798.

When did Finger Pulse Oximeter, Model: X1906P receive FDA 510(k) clearance?

Finger Pulse Oximeter, Model: X1906P received FDA 510(k) clearance on 2023-05-04, under 510(k) number K221798.

Who is the listed applicant for Finger Pulse Oximeter, Model: X1906P?

The FDA 510(k) record lists Shenzhen Changkun Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Finger Pulse Oximeter, Model: X1906P?

The FDA product code for Finger Pulse Oximeter, Model: X1906P is DQA.

列明Shenzhen Changkun Technology Co., Ltd.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。

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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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