FDA 510(k)

HemosIL D-二聚体HS 500

K号: K172903 · 2017-11-22

决定日期2017-11-22

产品代码DAP

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决定实质等同

器械摘要

HemosIL D-Dimer HS 500 is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 2017-11-22 under 510(k) number K172903. The device is classified under product code DAP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the HemosIL D-Dimer HS 500?

HemosIL D-Dimer HS 500 is a medical device that received FDA 510(k) clearance on 2017-11-22. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K172903.

When did HemosIL D-Dimer HS 500 receive FDA 510(k) clearance?

HemosIL D-Dimer HS 500 received FDA 510(k) clearance on 2017-11-22, under 510(k) number K172903.

Who is the listed applicant for HemosIL D-Dimer HS 500?

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

What is the FDA product code for HemosIL D-Dimer HS 500?

The FDA product code for HemosIL D-Dimer HS 500 is DAP.

列明Instrumentation Laboratory CO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。

K221359ACL TOP 970 CL, HemosIL CL 抗心磷脂IgM, HemosIL CL 抗ß2 糖蛋白-I IgM K223187HemosIL 液体抗-Xa K223090GEM Premier ChemSTAT K223402HemosIL von Willebrand 因子抗原 K213464HemosIL 液体抗-Xa K213426HemosIL ReadiPlasTin

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官方来源

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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。