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FDA 510(k)

CoolSculpting 系统

K号: K172144 · 2017-11-01

申请人Zeltiq Aesthetics
决定日期2017-11-01
产品代码OOK
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

CoolSculpting System is the device name listed in this FDA 510(k) record. The listed applicant is Zeltiq Aesthetics. It received FDA 510(k) clearance on 2017-11-01 under 510(k) number K172144. The device is classified under product code OOK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the CoolSculpting System?

CoolSculpting System is a medical device that received FDA 510(k) clearance on 2017-11-01. The listed applicant is Zeltiq Aesthetics. The 510(k) number is K172144.

When did CoolSculpting System receive FDA 510(k) clearance?

CoolSculpting System received FDA 510(k) clearance on 2017-11-01, under 510(k) number K172144.

Who is the listed applicant for CoolSculpting System?

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

What is the FDA product code for CoolSculpting System?

The FDA product code for CoolSculpting System is OOK.

相关临床试验

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。

NCT07608549FLASHPilot 1期安全性研究NOT_YET_RECRUITINGNCT06562205PAP系统外部临床研究（ECS）NOT_YET_RECRUITINGNCT06443177交感神经调节对动脉瘤性蛛网膜下腔出血继发脑动脉痉挛的影响SUSPENDEDNCT07095751人工智能辅助尿路摄像头评估系统，用于诊断膀胱癌NOT_YET_RECRUITING

相关器械（代码：OOK）

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。

K233732CoolSculpting Elite 系统Zeltiq Aesthetics, Inc. (Acquired by Allergan AestheticsK212707CoolSculpting Elite 系统Zeltiq Aesthetics, Inc.K193566ZELTIQ 冷冻溶脂系统Zeltiq Aesthetics, Inc.K183514ZELTIQ 冷冻溶脂系统Zeltiq Aesthetics, Inc.K181740ZELTIQ 冷冻溶脂系统Zeltiq Aesthetics, Inc.K171069ZELTIQ 冷冻溶脂系统Zeltiq Aesthetics, Inc.

官方来源

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