FDA 510(k)

Coretech 压缩系统 (Coretech RHB3003)

K号: K250817 · 2025-08-08

决定日期2025-08-08

产品代码JOW

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

Coretech Compression System (Coretech RHB3003) is the device name listed in this FDA 510(k) record. The listed applicant is Vive Health, LLC. It received FDA 510(k) clearance on 2025-08-08 under 510(k) number K250817. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Coretech Compression System (Coretech RHB3003)?

Coretech Compression System (Coretech RHB3003) is a medical device that received FDA 510(k) clearance on 2025-08-08. The listed applicant is Vive Health, LLC. The 510(k) number is K250817.

When did Coretech Compression System (Coretech RHB3003) receive FDA 510(k) clearance?

Coretech Compression System (Coretech RHB3003) received FDA 510(k) clearance on 2025-08-08, under 510(k) number K250817.

Who is the listed applicant for Coretech Compression System (Coretech RHB3003)?

The FDA 510(k) record lists Vive Health, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Coretech Compression System (Coretech RHB3003)?

The FDA product code for Coretech Compression System (Coretech RHB3003) is JOW.

列明Vive Health, 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。

K250729电动轮椅 (MOB1107)

官方来源

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