Cleared Traditional

MammoScreen? (3)

K240301 · Therapixel · Radiology

Aug 2024

Decision

182d

Days

Class 2

Risk

About This 510(k) Submission

K240301 is an FDA 510(k) clearance for the MammoScreen? (3), a Radiological Computer Assisted Detection/diagnosis Software For Lesions Suspicious For Cancer (Class II — Special Controls, product code QDQ), submitted by Therapixel (Nice, FR). The FDA issued a Cleared decision on August 1, 2024, 182 days after receiving the submission on February 1, 2024. This device falls under the Radiology review panel. Regulated under 21 CFR 892.2090.

Submission Details

510(k) Number	K240301 FDA.gov
FDA Decision	Cleared SESE
Date Received	February 01, 2024
Decision Date	August 01, 2024
Days to Decision	182 days
Submission Type	Traditional
Review Panel	Radiology (RA)
Summary	Summary PDF

Device Classification

Product Code	QDQ — Radiological Computer Assisted Detection/diagnosis Software For Lesions Suspicious For Cancer
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 892.2090
Definition	A Radiological Computer Assisted Detection And Diagnostic Software For Suspected Lesions Is An Image Processing Device Intended To Aid In The Detection, Localization, And Characterization Of Lesions Suspicious For Cancer On Acquired Medical Images (e.g., Mammography , Mr, Ct, Ultrasound, Radiography). The Device Detects, Identifies And Characterizes Lesions Suspicious For Cancer Based On Features Or Information Extracted From The Images, And May Provide Information About The Presence, Location, And Characteristics Of The Lesion To The User. Primary Diagnostic And Patient Management Decisions Are Made By The Clinical User.