Cleared Traditional

HealthCXR (K192320) - FDA 510(k) Clearance

Class II Radiology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K192320 · Zebra Medical Vision, Ltd. · Radiology device
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Nov 2019
Decision
92d
Days
Class 2
Risk

K192320 is an FDA 510(k) clearance for the HealthCXR. Classified as Radiological Computer-assisted Prioritization Software For Lesions (product code QFM), Class II - Special Controls.

Submitted by Zebra Medical Vision, Ltd. (Sefayim, IL). The FDA issued a Cleared decision on November 26, 2019 after a review of 92 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.2080 - the FDA radiology and imaging software oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Zebra Medical Vision, Ltd. devices

Submission Details

510(k) Number K192320 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 26, 2019
Decision Date November 26, 2019
Days to Decision 92 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
15d faster than avg
Panel avg: 107d · This submission: 92d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code QFM Radiological Computer-assisted Prioritization Software For Lesions
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.2080
Definition Radiological Computer-assisted Prioritization Software For Lesions 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.
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Radiology devices follow this clearance model.

Regulatory Peers - QFM Radiological Computer-assisted Prioritization Software For Lesions

All 39
Devices cleared under the same product code (QFM) and FDA review panel - the closest regulatory comparables to K192320.
HealthVCF
K192901 · Zebra Medical Vision, Ltd. · May 2020
AIMI-Triage CXR PTX
K193300 · Radlogics, Inc. · Apr 2020
Red Dot
K191556 · Behold.Ai Technologies Limited · Feb 2020
Critical Care Suite
K183182 · Ge Medical Systems, LLC · Aug 2019
HealthPNX
K190362 · Zebra Medical Vision, Ltd. · May 2019
cmTriage
K183285 · Curemetrix, Inc. · Mar 2019