Atlas FDA

Alinity m CMV

FDA 510(k) clearance K243485 · decided 2025-07-01

Clearance details

K-number
K243485
Device name
Alinity m CMV
Applicant
Abbott Molecular, Inc.
Decision
Substantially Equivalent
Date received
2024-11-08
Decision date
2025-07-01
Days to decision
235 days
Clearance type
Traditional
Product code
PAB
Device class
2
Regulation number
866.3180
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Des Plaines, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
cobas CMV (K252481)Roche Molecular Systems, Inc.2025-11-03
Aptima CMV Quant Assay (K243935)Hologic, Inc.2025-01-17

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
Alinity m HR HPV (P230003/S009)Abbott Molecular, Inc.2025-10-17
Alinity m HBV (P200013/S027)Abbott Molecular, Inc.2025-10-17
Alinity m HR HPV (P230003/S008)Abbott Molecular, Inc.2025-09-24
Alinity m HBV (P200013/S026)Abbott Molecular, Inc.2025-09-24
Alinity m HR HPV (P230003/S006)Abbott Molecular, Inc.2025-09-10
Vysis CLL Fish Probe Kit (P150041/S007)Abbott Molecular, Inc.2025-08-08
Vysis ALK Break Apart FISH Probe Kit (P110012/S022)Abbott Molecular, Inc.2025-08-05
Alinity m HR HPV (P230003/S007)Abbott Molecular, Inc.2025-04-18