Abbott Architect Havab-M

FDA 510(k) K063329 · Abbott Laboratories

Substantially Equivalent

510(k) numberK063329

Submission

Device name
Abbott Architect Havab-M
Applicant
Abbott Laboratories
Abbott Park, IL, US
Received
November 3, 2006
Decision date
April 16, 2007
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LOL – Hepatitis A Test (Antibody And Igm Antibody)
Device class
Class II (moderate risk)
Regulation
21 CFR 866.3310
Specialty
Microbiology

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K260048Elecsys Anti-HAV IgMLOL · Traditional Roche Diagnostics04/07/2026SE
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K243846Access anti-HAVLOL · Traditional Beckman Coulter, Inc.09/09/2025SE
K222850HAVAb IgG IILOL · Traditional Abbott Laboratories08/10/2023SE
K223403LIAISON Anti-HAV; LIAISON XSLOL · Special DiaSorin, Inc.12/09/2022SE
K210272LIAISON Anti-HAVLOL · Special DiaSorin, Inc.02/09/2021SE
K193532LIAISON Anti-HAV AssayLOL · Traditional DiaSorin, Inc.03/02/2020SE
K190428Elecsys Anti-HAV IILOL · Traditional Roche Diagnostics08/13/2019SE
K161964ADVIA Centaur HAV IgM AssayLOL · Traditional Siemens Healthcare Diagnostics, Inc.10/13/2016SE
K160650LIAISON HAV IgM, LIAISON Control HAV IgMLOL · Traditional DiaSorin, Inc.08/25/2016SE

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Questions and answers

When was Abbott Architect Havab-M cleared by the FDA?

Abbott Architect Havab-M (K063329) received a 510(k) decision of Substantially Equivalent on April 16, 2007, 164 days after the submission was received.

What is the product code of K063329?

The FDA product code is LOL – Hepatitis A Test (Antibody And Igm Antibody), a Class II (moderate risk) device regulated under 21 CFR 866.3310.