510(k) K082050

LIAISON HAV IGM ASSAY, LIAISON CONTROL HAV IGM by DiaSorin, Inc. — Product Code LOL

K082050 is an FDA 510(k) premarket notification submitted by DiaSorin, Inc. for the device "LIAISON HAV IGM ASSAY, LIAISON CONTROL HAV IGM". The FDA issued a decision of Substantially Equivalent on November 3, 2008. The device falls under product code LOL (Hepatitis A Test (Antibody And Igm Antibody)), a Class II device regulated under 21 CFR 866.3310. DiaSorin, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 3, 2008
Date Received
July 18, 2008
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Hepatitis A Test (Antibody And Igm Antibody)
Device Class
Class II
Regulation Number
866.3310
Review Panel
MI
Submission Type