FDA 510(k)

LIAISON Anti-HAV; LIAISON XS

K号: K223403 · 2022-12-09

决定日期2022-12-09

产品代码LOL

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决定实质等同

器械摘要

LIAISON Anti-HAV; LIAISON XS is the device name listed in this FDA 510(k) record. The listed applicant is DiaSorin, Inc.. It received FDA 510(k) clearance on 2022-12-09 under 510(k) number K223403. The device is classified under product code LOL. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the LIAISON Anti-HAV; LIAISON XS?

LIAISON Anti-HAV; LIAISON XS is a medical device that received FDA 510(k) clearance on 2022-12-09. The listed applicant is DiaSorin, Inc.. The 510(k) number is K223403.

When did LIAISON Anti-HAV; LIAISON XS receive FDA 510(k) clearance?

LIAISON Anti-HAV; LIAISON XS received FDA 510(k) clearance on 2022-12-09, under 510(k) number K223403.

Who is the listed applicant for LIAISON Anti-HAV; LIAISON XS?

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

What is the FDA product code for LIAISON Anti-HAV; LIAISON XS?

The FDA product code for LIAISON Anti-HAV; LIAISON XS is LOL.

列明DiaSorin, Inc.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。

K260770LIAISON Murex HBsAg Qual；LIAISON XL；LIAISON 稀释X K231214LIAISON VZV IgG HT，LIAISON 控制VZV IgG HT K213858LIAISON Calprotectin, LIAISON Q.S.E.T. Device Plus K213936LIAISON MeMed BV，LIAISON MeMed BV控制套件 K193650LIAISON Ferritin K202574LIAISON 疟原虫IgG，LIAISON 疟原虫IgG控制套件，LIAISON 疟原虫总抗体加

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