LIASYS 600电解质测量系统,LIASYS 600肌酐试剂,LIASYS 600
K号: K172232 · 2019-06-12
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器械摘要
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.
相关临床试验
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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。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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