FDA 510(k)

Stryker CrossFlow 日用流入 cassette 管道和患者用管道

K号: K151932 · 2016-03-31

决定日期2016-03-31

产品代码HRX

咨询委员会OR 请注意，由于原文中未提供具体的医疗设备监管文本，以下是一个示例翻译，您可以根据实际文本进行调整： --- 产品名称：[产品名称] 公司名称：[公司名称] 根据FDA 510(k)预市场批准程序，[产品名称]已获得批准，用于[产品用途描述]。产品注册号：[注册号] PMA编号：[PMA编号] 临床试验编号（NCT）：[NCT编号] PubMed ID（PMID）：[PMID编号] 更多信息请访问以下链接： [URL] --- 请将上述示例中的[产品名称]、[公司名称]、[注册号]、[PMA编号]、[NCT编号]、[PMID编号]和[URL]替换为实际的文本内容。

决定实质等同

器械摘要

Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corporation. It received FDA 510(k) clearance on 2016-03-31 under 510(k) number K151932. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing?

Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing is a medical device that received FDA 510(k) clearance on 2016-03-31. The listed applicant is Stryker Corporation. The 510(k) number is K151932.

When did Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing receive FDA 510(k) clearance?

Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing received FDA 510(k) clearance on 2016-03-31, under 510(k) number K151932.

Who is the listed applicant for Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing?

The FDA 510(k) record lists Stryker Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing?

The FDA product code for Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing is HRX.

列明Stryker 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。

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