FDA 510(k)

KIDS动脉过滤器

K号: K242953 · 2024-12-20

决定日期2024-12-20

产品代码DTM

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

KIDS Arterial Filters is the device name listed in this FDA 510(k) record. The listed applicant is Sorin Group Italia S.R.L.. It received FDA 510(k) clearance on 2024-12-20 under 510(k) number K242953. The device is classified under product code DTM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the KIDS Arterial Filters?

KIDS Arterial Filters is a medical device that received FDA 510(k) clearance on 2024-12-20. The listed applicant is Sorin Group Italia S.R.L.. The 510(k) number is K242953.

When did KIDS Arterial Filters receive FDA 510(k) clearance?

KIDS Arterial Filters received FDA 510(k) clearance on 2024-12-20, under 510(k) number K242953.

Who is the listed applicant for KIDS Arterial Filters?

The FDA 510(k) record lists Sorin Group Italia S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KIDS Arterial Filters?

The FDA product code for KIDS Arterial Filters is DTM.

列明Sorin Group Italia S.R.L.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。

K253671双阶段静脉导管 K251783Inspire HCR和HCR DUAL心脏切开储液器 K253616ProtekDilate 血管通路套件 K250610Easyflow (103-200; 103-300); Easyflow Duo (103-210; 103-310)K250150VANGUARD 血液心肌保护系统（Vanguard 4:1 血液心肌保护套装）；VANGUARD 血液心肌保护系统（Vanguard 4:1 血液心肌保护套装带分流）；VANGUARD 血液心肌保护系统（Vanguard 4:1 血液心肌保护套装迷你版）K243264DHF 0.2 血液浓缩器（DHF 02）；DHF 0.6 血液浓缩器（DHF 06）；SH 14 血液浓缩器（SH 14）

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