Atlas FDA

Alinity m HBV

FDA premarket approval P200013/S010 · decided 2023-02-21

Approval details

PMA number
P200013
Supplement
S010
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Alinity m HBV
Generic name
Hepatitis Viral B DNA Detection
Applicant
Abbott Molecular, Inc.
Date received
2022-12-02
Decision date
2023-02-21
Days to decision
81 days
Decision code
APPR
Product code
MKT
Advisory committee
Microbiology
Expedited review
No
Location
Des Plaines, IL
Statement
Approval to release software version 1.7.1 in the US.

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510(k) clearances by this applicant

RecordFirmDate
Alinity m HCV (K252102)Abbott Molecular, Inc.2025-09-25
Alinity m EBV (09N43-095) (K243489)Abbott Molecular, Inc.2025-07-28
Alinity m CMV (K243485)Abbott Molecular, Inc.2025-07-01
Alinity m BKV (K241921)Abbott Molecular, Inc.2025-03-24
Alinity m Resp-4-Plex (K241573)Abbott Molecular, Inc.2025-02-14
Alinity m HSV 1 & 2 / VZV (K233349)Abbott Molecular, Inc.2024-05-03
Alinity m STI Assay (K222379)Abbott Molecular, Inc.2023-03-03
Alinity m EBV AMP Kit (List No. 09N43-095), Alinity m EBV CTRL Kit (List No. 09N43-085), Alinity m EBV CAL Kit (List No. 09N43-075) (K212778)Abbott Molecular, Inc.2022-07-15