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Alinity i HBsAg Next Qualitative assay, Alinity i HBsAg Next Confirmatory assay

FDA premarket approval P210003/S006 · decided 2023-09-28

Approval details

PMA number
P210003
Supplement
S006
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Alinity i HBsAg Next Qualitative assay, Alinity i HBsAg Next Confirmatory assay
Generic name
Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)
Applicant
Abbott Laboratories
Date received
2023-04-03
Decision date
2023-09-28
Days to decision
178 days
Decision code
APPR
Product code
LOM
Advisory committee
Microbiology
Expedited review
No
Location
Abbott Park, IL
Statement
Approval for the Migration of the Abbott ARCHITECT HBsAg Next Qualitative and ARCHITECT HBsAg Next Confirmatory assay (P210003) to the Alinity i system (referred to as the Alinity i analyzer), which will be known as the Alinity i HBsAg Next Qualitative and Alinity i HBsAg Next Confirmatory assay.

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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