Atlas FDA

SOMO.V ABUS (AUTOMATED BREAST ULTRASOUND SYSTEM)

FDA premarket approval P110006 · decided 2012-09-18

Approval details

PMA number
P110006
Trade name
SOMO.V ABUS (AUTOMATED BREAST ULTRASOUND SYSTEM)
Generic name
Automated breast ultrasound
Applicant
GE Healthcare
Date received
2011-02-11
Decision date
2012-09-18
Days to decision
585 days
Decision code
APPR
Product code
PAA
Advisory committee
Radiology
Expedited review
No
Location
Wauwatosa, WI
Statement
APPROVAL FOR THE SOMO-V: AUTOMATED BREAST ULTRASOUND SYSTEM (ABUS). THIS DEVICE IS INDICATED AS AN ADJUNCT TO MAMMOGRAPHY FOR BREAST CANCER SCREENING IN ASYMPTOMATIC WOMEN FOR WHOM SCREENINGMAMMOGRAPHY FINDINGS ARE NORMAL OR BENIGN (BI-RADS ASSESSMENT CATEGORY 1 OR 2), WITH DENSE BREAST PARENCHYMA (BI-RADS COMPOSITION/DENSITY 3 OR 4) AND HAVE NOT HAD PREVIOUS CLINICALBREAST INTERVENTION. THE DEVICE IS INTENDED TO INCREASE BREAST CANCER DETECTION IN THE DESCRIBED PATIENT POPULATION.

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510(k) clearances by this applicant

RecordFirmDate
View (K253639)GE Healthcare2026-01-08
MR Contour DL (K242925)GE Healthcare2025-04-01
Digital Expert Access with Remote Scanning (K232346)GE Healthcare2023-10-27
Precision DL (K223212)GE Healthcare2023-04-27
Xeleris V Processing and Review System (K221680)GE Healthcare2023-03-01
Omni Legend (K221932)GE Healthcare2022-09-02
Voluson P6, Voluson P8 (K213689)GE Healthcare2022-02-17
Voluson S6, Voluson S8, Voluson S8t, Voluson S10, Voluson S10 Expert (K213642)GE Healthcare2022-01-13