FDA 510(k)

Optimos® 膀胱切开刀

K号: K223256 · 2023-04-05

决定日期2023-04-05

产品代码KNS

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决定实质等同

器械摘要

Optimos™ Cystotome is the device name listed in this FDA 510(k) record. The listed applicant is Taewoong Medical Co., Ltd.. It received FDA 510(k) clearance on 2023-04-05 under 510(k) number K223256. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Optimos™ Cystotome?

Optimos™ Cystotome is a medical device that received FDA 510(k) clearance on 2023-04-05. The listed applicant is Taewoong Medical Co., Ltd.. The 510(k) number is K223256.

When did Optimos™ Cystotome receive FDA 510(k) clearance?

Optimos™ Cystotome received FDA 510(k) clearance on 2023-04-05, under 510(k) number K223256.

Who is the listed applicant for Optimos™ Cystotome?

The FDA 510(k) record lists Taewoong Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Optimos™ Cystotome?

The FDA product code for Optimos™ Cystotome is KNS.

列明Taewoong Medical Co., Ltd.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。

K260962Sphincterotome K252648Niti-S SPAXUS 支架 K251123Niti-S 胆道支架; Niti-S 胆道细 M 支架 K243619Niti-S 食管支架; 食管 TTS 支架 K250663Niti-S 十二指肠舒适支架，Niti-S 结肠舒适支架 K223067Niti-S 十二指肠支架; Niti-S 结肠舒适支架

查看所有 11 个设备 →

相关器械（代码：KNS）

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。

K262460Rezum系统Boston Scientific K260962SphincterotomeTaewoong Medical Co., Ltd.K252388征服水蒸气消融装置Francis Medical, Inc.K252889一次性3腔针刀V（KD-V441M，KD-V451M）Olympus Medical Systems Corporation K250945一次性预装括约肌刀V（远端导丝引导）（KD-VC600系列）；一次性括约肌刀V（远端导丝引导）（KD-VC400系列）；一次性三腔括约肌刀（KD-V系列）；一次性三腔括约肌刀（KD系列）Olympus Medical Systems Corp.K250351一次性电外科刀 (KD-612L, KD-612U)；一次性电外科刀 (KD-620UR)；一次性电外科刀 (KD-650L, KD-650U)Olympus Medical Systems Corporation

官方来源

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