FDA 510(k)

ONLINE TDM 万古霉素 Gen.3

K号: K152245 · 2016-01-08

决定日期2016-01-08

产品代码LEH

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决定实质等同

器械摘要

ONLINE TDM Vancomycin Gen.3 is the device name listed in this FDA 510(k) record. The listed applicant is Roche Diagnostics Operations (Rdo). It received FDA 510(k) clearance on 2016-01-08 under 510(k) number K152245. The device is classified under product code LEH. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ONLINE TDM Vancomycin Gen.3?

ONLINE TDM Vancomycin Gen.3 is a medical device that received FDA 510(k) clearance on 2016-01-08. The listed applicant is Roche Diagnostics Operations (Rdo). The 510(k) number is K152245.

When did ONLINE TDM Vancomycin Gen.3 receive FDA 510(k) clearance?

ONLINE TDM Vancomycin Gen.3 received FDA 510(k) clearance on 2016-01-08, under 510(k) number K152245.

Who is the listed applicant for ONLINE TDM Vancomycin Gen.3?

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

What is the FDA product code for ONLINE TDM Vancomycin Gen.3?

The FDA product code for ONLINE TDM Vancomycin Gen.3 is LEH.

列明Roche Diagnostics Operations (Rdo)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。

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官方来源

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