← FDA DEVICE PRODUCT CODES

FDA PRODUCT CODE · CLASS II

QASRadiological Computer-Assisted Triage And Notification Software

Radiological computer-assisted triage and notification software is an image processing device intended to aid in prioritization and triage of time sensitive patient detection and diagnosis based on the analysis of medical images acquired from radiological signal acquisition systems. The device identifies or prioritizes time sensitive imaging for review by prespecified clinical users based on software-based image analysis but does not provide information from the image analysis other than triage and notification .

DEVICE CLASS
Class II
REGULATION
21 CFR 892.2080
MEDICAL SPECIALTY
Radiology
REVIEW PANEL
RA
ImplantLife-sustainingGMP-exemptThird-party review eligible
29
510(K)/PMA CLEARANCES
510k: 29
0
RECALL ENTRIES

Recent clearances

K261085iSchemaview · 510k2026-07-13
K260729GuideAI Health · 510k2026-06-18
K261317Aidoc Medical , Ltd. · 510k2026-05-14
K253163Ever Fortune.Ai, Co., Ltd. · 510k2026-04-22
K252421JLK, Inc. · 510k2026-03-24
K253818Harrison-AI Medical Pty, Ltd. · 510k2026-03-03
K253578Aidoc Medical , Ltd. · 510k2026-02-26
K251195Aidoc Medical , Ltd. · 510k2026-01-27

Related on SPEQ

Medical devices industryMedical device quality (ISO 13485)FDA device clearancesFDA enforcement & recalls

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

Weekly Briefing

Get the Weekly GxP Briefing

Curated regulatory intelligence — enforcement, recalls, guidance, and quality signals — in one practitioner-grade email each week. Free.

Read a past issue →