FDA 510(k)

ThermAffyx™ 患者安全系统

K号: K260278 · 2026-07-08

决定日期2026-07-08

产品代码DWJ

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

ThermAffyx(TM) Patient Safety System is the device name listed in this FDA 510(k) record. The listed applicant is Stihler Electronic GmbH. It received FDA 510(k) clearance on 2026-07-08 under 510(k) number K260278. The device is classified under product code DWJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ThermAffyx(TM) Patient Safety System?

ThermAffyx(TM) Patient Safety System is a medical device that received FDA 510(k) clearance on 2026-07-08. The listed applicant is Stihler Electronic GmbH. The 510(k) number is K260278.

When did ThermAffyx(TM) Patient Safety System receive FDA 510(k) clearance?

ThermAffyx(TM) Patient Safety System received FDA 510(k) clearance on 2026-07-08, under 510(k) number K260278.

Who is the listed applicant for ThermAffyx(TM) Patient Safety System?

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

What is the FDA product code for ThermAffyx(TM) Patient Safety System?

The FDA product code for ThermAffyx(TM) Patient Safety System is DWJ.

列明Stihler Electronic GmbH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。

K202197Astopad 患者保暖系统

官方来源

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