Atlas FDA

ARCHITECT CORE / Alinity i Anti-HBc

FDA premarket approval P080023/S040 · decided 2023-10-11

Approval details

PMA number
P080023
Supplement
S040
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
ARCHITECT CORE / Alinity i Anti-HBc
Generic name
Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)
Applicant
Abbott Laboratories
Date received
2023-05-08
Decision date
2023-10-11
Days to decision
156 days
Decision code
APPR
Product code
LOM
Advisory committee
Microbiology
Expedited review
No
Location
Abbott Park, IL
Statement
Approval for the formulation change for the common accessories Pre-Trigger and Trigger, and storage condition changes for Pre-Trigger, used on ARCHITECT i2000SR, ARCHITECT i1000SR and Alinity i analyzer.

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510(k) clearances by this applicant

RecordFirmDate
Anti-HCV Next (K252424)Abbott Laboratories2026-04-28
ARCHITECT iGentamicin (K243500)Abbott Laboratories2025-07-09
Alinity i Rubella IgG (K243168)Abbott Laboratories2025-06-20
Alinity h-series System (K243283)Abbott Laboratories2025-02-20
Alinity i Toxo IgM (K233932)Abbott Laboratories2024-08-30
TBI (K232669)Abbott Laboratories2023-09-29
HAVAb IgG II (K222850)Abbott Laboratories2023-08-10
Alinity h-series System (K220031)Abbott Laboratories2023-08-04