510(k) K243846

Access anti-HAV by Beckman Coulter, Inc. — Product Code LOL

K243846 is an FDA 510(k) premarket notification submitted by Beckman Coulter, Inc. for the device "Access anti-HAV". The FDA issued a decision of Substantially Equivalent on September 9, 2025. The device falls under product code LOL (Hepatitis A Test (Antibody And Igm Antibody)), a Class II device regulated under 21 CFR 866.3310. Beckman Coulter, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 9, 2025
Date Received
December 16, 2024
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