FDA 510(k)

ETEST吉普他汀（GEP）（0.016-256 µg/mL）

K号: K260447 · 2026-04-21

决定日期2026-04-21

产品代码JWY

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决定实质等同

器械摘要

ETEST Gepotidacin (GEP) (0.016-256 µg/mL) is the device name listed in this FDA 510(k) record. The listed applicant is bioMérieux SA. It received FDA 510(k) clearance on 2026-04-21 under 510(k) number K260447. The device is classified under product code JWY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ETEST Gepotidacin (GEP) (0.016-256 µg/mL)?

ETEST Gepotidacin (GEP) (0.016-256 µg/mL) is a medical device that received FDA 510(k) clearance on 2026-04-21. The listed applicant is bioMérieux SA. The 510(k) number is K260447.

When did ETEST Gepotidacin (GEP) (0.016-256 µg/mL) receive FDA 510(k) clearance?

ETEST Gepotidacin (GEP) (0.016-256 µg/mL) received FDA 510(k) clearance on 2026-04-21, under 510(k) number K260447.

Who is the listed applicant for ETEST Gepotidacin (GEP) (0.016-256 µg/mL)?

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

What is the FDA product code for ETEST Gepotidacin (GEP) (0.016-256 µg/mL)?

The FDA product code for ETEST Gepotidacin (GEP) (0.016-256 µg/mL) is JWY.

列明bioMérieux SA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。

K210793VIDAS 肾功能检测 K200512ETEST普拉茚胺（PLZ）（0.016-256 µg/mL）

相关器械（代码：JWY）

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。

K260696MTS 丙硫异烟胺 0.016-256 µg/mLLiofilchem s.r.l.K252114MTS 阿齐霉素-阿维巴坦 0.016/4 - 256/4 µg/mLLiofilchem s.r.l.K252062Sensititre 18-24小时MIC或断裂点敏感性系统，含多粘菌素，稀释范围为0.12-16 μg/mL。Thermo Fisher Scientific K250575Sensititre 18-24小时MIC或断裂点敏感性系统，含阿奇霉素/阿维巴坦，稀释范围为0.008/4 - 64/4 μg/mL。Thermo Fisher Scientific K252014Sensititre 18-24小时MIC或断裂点敏感性系统，含阿米卡星，稀释范围为0.25-256 μg/mL。Thermo Fisher Scientific K251580MTS 氨苄西林-杜洛巴坦 0.004/4 - 64/4 µg/mL (SUD)Liofilchem s.r.l.

官方来源

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