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Aptima CMV Quant Assay

FDA premarket approval P210029/S001 · decided 2022-07-20

Approval details

PMA number
P210029
Supplement
S001
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Aptima CMV Quant Assay
Generic name
Cytomegalovirus (cmv) dna quantitative assay
Applicant
Hologic, Inc.
Date received
2022-06-16
Decision date
2022-07-20
Days to decision
34 days
Decision code
OK30
Product code
PAB
Advisory committee
Microbiology
Expedited review
No
Location
San Diego, CA
Statement
Add additional monitoring and final release criteria.

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510(k) clearances by this applicant

RecordFirmDate
CoolSeal Generator® (CSL-200-90) (K253634)Hologic, Inc.2026-06-17
Panther Fusion GI Expanded Bacterial Assay (K251993)Hologic, Inc.2025-09-25
Genius AI Detection 2.0 (K243341)Hologic, Inc.2025-07-31
Aptima SARS-CoV-2 Assay (K243396)Hologic, Inc.2025-02-13
Aptima CMV Quant Assay (K243935)Hologic, Inc.2025-01-17
Aptima BV Assay; Aptima CV/TV Assay (K243345)Hologic, Inc.2024-11-25
Panther Fusion SARS-CoV-2/Flu A/B/RSV assay (K242465)Hologic, Inc.2024-11-15
Fluent Pro Fluid Management System (FLT-200); Fluent Pro Fluid Management System Disposable Procedure Kit (6-pack) (FLT-212); Fluent Pro Fluid Management System Disposable Procedure Kit (1-pack) (FLT-212S); Fluent Pro Fluid Management System Tissue Trap Multipack (10-pack) (FLT-210); Fluent Pro Fluid Management System Waste Bag Multipack (5-pack) (FLT-205) (K240886)Hologic, Inc.2024-07-25