FDA 510(k)

Aurora 吸出器

K号: K190075 · 2019-02-12

决定日期2019-02-12

产品代码GEI

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决定实质等同

器械摘要

Aurora Evacuator is the device name listed in this FDA 510(k) record. The listed applicant is Rebound Therapeutics. It received FDA 510(k) clearance on 2019-02-12 under 510(k) number K190075. 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 Aurora Evacuator?

Aurora Evacuator is a medical device that received FDA 510(k) clearance on 2019-02-12. The listed applicant is Rebound Therapeutics. The 510(k) number is K190075.

When did Aurora Evacuator receive FDA 510(k) clearance?

Aurora Evacuator received FDA 510(k) clearance on 2019-02-12, under 510(k) number K190075.

Who is the listed applicant for Aurora Evacuator?

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

What is the FDA product code for Aurora Evacuator?

The FDA product code for Aurora Evacuator is GEI.

列明Rebound Therapeutics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。

K203745AURORA Evacuator +Coag K201840Aurora 手术显微镜系统（Surgiscope），Aurora 手术显微镜系统（图像控制盒）K201637Aurora 吸出器 + 凝固 K191861Aurora 手术显微镜系统 K180372Aurora 吸出器

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.

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