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FDA 510(k)

LIASYS 600电解质测量系统,LIASYS 600肌酐试剂,LIASYS 600

K号: K172232 · 2019-06-12

决定日期2019-06-12
产品代码JGS
咨询委员会CH 请注意,您提供的文本“CH”不足以进行翻译。请提供完整的医疗设备监管文本,以便我能够进行准确的翻译。
决定实质等同

器械摘要

LIASYS 600 Electrolyte Measurement System, LIASYS 600 Creatinine reagent, LIASYS 600 is the device name listed in this FDA 510(k) record. The listed applicant is Ams Diagnostics. It received FDA 510(k) clearance on 2019-06-12 under 510(k) number K172232. The device is classified under product code JGS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the LIASYS 600 Electrolyte Measurement System, LIASYS 600 Creatinine reagent, LIASYS 600?

LIASYS 600 Electrolyte Measurement System, LIASYS 600 Creatinine reagent, LIASYS 600 is a medical device that received FDA 510(k) clearance on 2019-06-12. The listed applicant is Ams Diagnostics. The 510(k) number is K172232.

When did LIASYS 600 Electrolyte Measurement System, LIASYS 600 Creatinine reagent, LIASYS 600 receive FDA 510(k) clearance?

LIASYS 600 Electrolyte Measurement System, LIASYS 600 Creatinine reagent, LIASYS 600 received FDA 510(k) clearance on 2019-06-12, under 510(k) number K172232.

Who is the listed applicant for LIASYS 600 Electrolyte Measurement System, LIASYS 600 Creatinine reagent, LIASYS 600?

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

What is the FDA product code for LIASYS 600 Electrolyte Measurement System, LIASYS 600 Creatinine reagent, LIASYS 600?

The FDA product code for LIASYS 600 Electrolyte Measurement System, LIASYS 600 Creatinine reagent, LIASYS 600 is JGS.

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相关器械(代码:JGS)

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。

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