FDA 510(k)

双极电极 CELON ProCurve V

K号: K172535 · 2017-11-16

决定日期2017-11-16

产品代码GEI

咨询委员会SU 请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。

决定实质等同

器械摘要

Bipolar applicator CELON ProCurve V is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Winter & Ibe GmbH. It received FDA 510(k) clearance on 2017-11-16 under 510(k) number K172535. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Bipolar applicator CELON ProCurve V?

Bipolar applicator CELON ProCurve V is a medical device that received FDA 510(k) clearance on 2017-11-16. The listed applicant is Olympus Winter & Ibe GmbH. The 510(k) number is K172535.

When did Bipolar applicator CELON ProCurve V receive FDA 510(k) clearance?

Bipolar applicator CELON ProCurve V received FDA 510(k) clearance on 2017-11-16, under 510(k) number K172535.

Who is the listed applicant for Bipolar applicator CELON ProCurve V?

The FDA 510(k) record lists Olympus Winter & Ibe GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Bipolar applicator CELON ProCurve V?

The FDA product code for Bipolar applicator CELON ProCurve V is GEI.

列明Olympus Winter & Ibe 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。

K260649OES ELITE 球囊内镜及其附件；球囊，17 Fr. (WA2C17BO)；球囊，19.8 Fr. (WA2C19BO)；球囊，21 Fr. (WA2C21BO)；球囊，21 Fr.，用于带斜坡的套管 (WA2C21RO)；球囊，21 Fr.，长 (WA2C21LO)；球囊，21 Fr.，用于直型套管 (WA2C21SO)；球囊，22.5 Fr. (WA2C22BO)；球囊，25 Fr. (WA2C25BO)；光学球囊，19.8 Fr. (WA2C19BV)；光学球囊，21 Fr. (WA2C21BV)；光学球囊，21 Fr.，用于直型套管 (WA2C21SV)；光学球囊，K252043双极治疗仪CelonProBreath (WB990310)；双极治疗仪CelonProSleep plus (WB990311)；双极治疗仪CelonProBreath (WB990210)；双极治疗仪CelonProSleep plus (WB990211)K231777电外科手术发生器 ESG-410 及附件（WA91327U，WA91327W），附件：脚踏开关（WA91311W，WA91321W）K221522HF-cables（可重复使用）K223183光导电缆 K213207套管，旋塞附件

查看所有 22 个设备 →

相关器械（代码：GEI）

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。

K254196HARMONIC 1100 剪刀（HAR1120）；HARMONIC 1100 剪刀（HAR1136）Ethicon Endo-Surgery, LLC K261959Neptune® SafeAir® 10英尺烟雾排放笔，方形涂层，70mm刀片，推钮开关（0703-046-100）；Neptune® SafeAir® 10英尺烟雾排放笔，方形涂层，推钮开关，大批量非无菌（0703-046-102）；Neptune® SafeAir® 10英尺烟雾排放笔，方形涂层，70mm刀片，旋转开关（0703-047-100）；Neptune® SafeAir® 10英尺烟雾排放笔，方形涂层，旋转开关，大批量非无菌（0703-047-102）Stryker Instruments K261070LigaSure™ RAS 马里兰州颚部血管封合/分割器，纳米涂层Covidien, LLC K254185Potenza PrimeJeisys Medical Incorporated K262364艾利安谜团射频设备Ellian Corp K253859Scarlet Pro（Scarlet Pro）VIOL Co., Ltd.

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。