FDA 510(k)

Denali™ 下腔静脉滤过系统 – 髂股部和颈静脉/锁骨下输送套件

K号: K240257 · 2024-02-29

申请人Bd

决定日期2024-02-29

产品代码DTK

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

Denali™ Vena Cava Filter System – Femoral and Jugular/Subclavian Delivery Kit is the device name listed in this FDA 510(k) record. The listed applicant is Bd. It received FDA 510(k) clearance on 2024-02-29 under 510(k) number K240257. The device is classified under product code DTK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Denali™ Vena Cava Filter System – Femoral and Jugular/Subclavian Delivery Kit?

Denali™ Vena Cava Filter System – Femoral and Jugular/Subclavian Delivery Kit is a medical device that received FDA 510(k) clearance on 2024-02-29. The listed applicant is Bd. The 510(k) number is K240257.

When did Denali™ Vena Cava Filter System – Femoral and Jugular/Subclavian Delivery Kit receive FDA 510(k) clearance?

Denali™ Vena Cava Filter System – Femoral and Jugular/Subclavian Delivery Kit received FDA 510(k) clearance on 2024-02-29, under 510(k) number K240257.

Who is the listed applicant for Denali™ Vena Cava Filter System – Femoral and Jugular/Subclavian Delivery Kit?

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

What is the FDA product code for Denali™ Vena Cava Filter System – Femoral and Jugular/Subclavian Delivery Kit?

The FDA product code for Denali™ Vena Cava Filter System – Femoral and Jugular/Subclavian Delivery Kit is DTK.

列明Bd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。

K253445BD Surgiphor™ 1000 mL 抗菌冲洗系统 (910120)K232434BD Veritor™ System for Rapid Detection of Flu A+B CLIA Waived Kit K223016BD VeritorTM System for Rapid Detection of Flu A+B CLIA-Waived Kit K221504BD Surgiphor™ 抗菌冲洗系统 K180438BD Veritor System for Rapid Detection of Flu A + B CLIA waived kit

相关器械（代码：DTK）

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。

K242612Option ELITE 下腔静脉滤过系统 (352506070E 352506100E)Argon Medical Devices, Inc.K240578VenaTech® LP 腔静脉滤器系统和 VenaTech® 可转换腔静脉滤器系统B.Braun Medical, Inc.K241507ALN 可选下腔静脉滤器 (FB.010500, FF.010995, FJ.120096, FB.HOOK, FF.HOOK, FJ.HOOK)Aln S.A.R.L.K233680Celect Platinum 股静脉滤器套装 (IGTCFS-65-1-FEM-CELECT-PT); Celect Platinum 颈静脉滤器套装 (IGTCFS-65-1-JUG-CELECT-PT); Celect Platinum 股静脉和颈静脉滤器套装 (IGTCFS-65-1-UNI-CELECT-PT); Günther Tulip 股静脉滤器套装 (IGTCFS-65-1-FEM-TULIP); Günther Tulip 颈静脉滤器套装 (IGTCFS-65-1-JUG-TULIP); Günther Tulip 静脉滤器William Cook Europe Aps K211874Günther Tulip Vena Cava Filter Set for Femoral Vein Approach, Günther Tulip Vena Cava Filter Set for Jugular Vein Approach, Günther Tulip Vena Cava Filter Set for Femoral and Jugular Vein ApproachWilliam Cook Europe Aps K211875Cook Celect Platinum 股静脉途径下腔静脉滤器套装，Cook Celect Platinum 颈静脉途径下腔静脉滤器套装，Cook Celect Platinum 股静脉和颈静脉途径下腔静脉滤器套装William Cook Europe Aps

官方来源

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