Atlas FDA

Abbott RealTime IDH1

FDA premarket approval P170041/S007 · decided 2023-10-24

Approval details

PMA number
P170041
Supplement
S007
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
Abbott RealTime IDH1
Generic name
Somatic gene mutation detection system
Applicant
Abbott Molecular, Inc.
Date received
2023-06-27
Decision date
2023-10-24
Days to decision
119 days
Decision code
APPR
Product code
OWD
Advisory committee
Medical Genetics
Expedited review
No
Location
Des Plaines, IL
Statement
Approval for expanding the indication for use of Abbott RealTime IDH1 as an aid in identifying myelodysplastic syndrome (MDS) patients with isocitrate dehydrogenase-1 (IDH1) mutation for treatment with TIBSOVO® (ivosidenib).

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510(k) clearances by this applicant

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Alinity m HCV (K252102)Abbott Molecular, Inc.2025-09-25
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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