Perifix and Contiplex Catheter
K号: K153297 · 2016-08-12
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器械摘要
Perifix and Contiplex Catheter is the device name listed in this FDA 510(k) record. The listed applicant is B.Braun Medical, Inc.. It received FDA 510(k) clearance on 2016-08-12 under 510(k) number K153297. The device is classified under product code BSO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Perifix and Contiplex Catheter?
Perifix and Contiplex Catheter is a medical device that received FDA 510(k) clearance on 2016-08-12. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K153297.
When did Perifix and Contiplex Catheter receive FDA 510(k) clearance?
Perifix and Contiplex Catheter received FDA 510(k) clearance on 2016-08-12, under 510(k) number K153297.
Who is the listed applicant for Perifix and Contiplex Catheter?
The FDA 510(k) record lists B.Braun Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Perifix and Contiplex Catheter?
The FDA product code for Perifix and Contiplex Catheter is BSO.
相关临床试验
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列明B.Braun Medical, Inc.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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相关器械（代码：BSO）
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。
K241410EDEN ControlCathJmt Co., Ltd.K231242Perifix FX Catheter; Contiplex FX CatheterB.Braun Medical, Inc.K230603Arrow Non-Stimulating SnapLock Adapter (K-05520-005C); Arrow Non-Stimulating Next Gen SnapLock Adapter (Luer Connection) (CA-000010-19); Arrow Non-Stimulating Next Gen SnapLock Adapter (Neuraxial Connection) (CA-000014-19); Arrow Stimulating SnapLock Adapter (with cable) (TZ-02060-001); Arrow Stimulating SnapLock Adapter (with tab) (TZ-05000-002)Teleflex MedicalK193664SubQKath Catheter and Needle SetHk SurgicalK200624Percutaneous IntroducerEpimed International, Inc.K191470C-CAT Anaesthesia Catheter kitCimpax Aps
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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