Atlas FDA

Alinity m HR HPV Assay

FDA premarket approval P230003/S005 · decided 2024-09-05

Approval details

PMA number
P230003
Supplement
S005
Supplement type
Special (Immediate Track)
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
Alinity m HR HPV Assay
Generic name
KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS
Applicant
Abbott Molecular, Inc.
Date received
2024-08-08
Decision date
2024-09-05
Days to decision
28 days
Decision code
APPR
Product code
MAQ
Advisory committee
Microbiology
Expedited review
No
Location
Des Plaines, IL
Statement
Approval to the request to include sample tube label requirements and edits to the the instrument Operations Manual Addendum.

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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