FDA 510(k)

POTENZA

K号: K231216 · 2024-12-10

决定日期2024-12-10

产品代码GEI

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决定实质等同

器械摘要

POTENZA is the device name listed in this FDA 510(k) record. The listed applicant is Jeisys Medical, Inc.. It received FDA 510(k) clearance on 2024-12-10 under 510(k) number K231216. 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 POTENZA?

POTENZA is a medical device that received FDA 510(k) clearance on 2024-12-10. The listed applicant is Jeisys Medical, Inc.. The 510(k) number is K231216.

When did POTENZA receive FDA 510(k) clearance?

POTENZA received FDA 510(k) clearance on 2024-12-10, under 510(k) number K231216.

Who is the listed applicant for POTENZA?

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

What is the FDA product code for POTENZA?

The FDA product code for POTENZA is GEI.

列明Jeisys 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。

K231287POTENZA K230663密度 K223685SmoothCool HR 系统 K213484SmoothCool HR 系统 K201685Potenza K183284INTRAcel RF Microneedle System

查看所有 10 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

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