Cleared Traditional

K253244 - AirRay-mini 80A

K253244 is an FDA 510(k) clearance for AirRay-mini 80A, manufactured by Poskom Co., Ltd.. The device is a Class 2 Radiology device with product code IZL cleared through the Traditional 510(k) pathway after a 147-day FDA review.

K253244 · Poskom Co., Ltd. · Radiology device
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Feb 2026
Decision
147d
Days
Class 2
Risk

K253244 is an FDA 510(k) clearance for the AirRay-mini 80A, AirRay-mini 90A, AirRay-mini 80F, AirRay-mini 90F (AirRay-mini). Classified as System, X-ray, Mobile (product code IZL), Class II - Special Controls.

Submitted by Poskom Co., Ltd. (Gyeonggi-Do, KR). The FDA issued a Cleared decision on February 23, 2026 after a review of 147 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1720 - 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 Poskom Co., Ltd. devices

FDA 510(k) Submission Details - K253244

510(k) Number K253244 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 29, 2025
Decision Date February 23, 2026
Days to Decision 147 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
40d slower than avg
Panel avg: 107d · This submission: 147d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IZL Device Classification - Class 2, Special Controls

Product Code IZL System, X-ray, Mobile
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1720
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 - IZL System, X-ray, Mobile

All 130
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