Cleared Traditional

K052341 - AJEX 9015/135H PORTABLE X-RAY

K052341 is an FDA 510(k) clearance for AJEX 9015/135H PORTABLE X-RAY, manufactured by Jpi America, Inc.. The device is a Class 2 Radiology device with product code IZL cleared through the Traditional 510(k) pathway after a 42-day FDA review.

K052341 · Jpi America, Inc. · Radiology device
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Oct 2005
Decision
42d
Days
Class 2
Risk

K052341 is an FDA 510(k) clearance for the AJEX 9015/135H PORTABLE X-RAY. Classified as System, X-ray, Mobile (product code IZL), Class II - Special Controls.

Submitted by Jpi America, Inc. (Farmingdale, US). The FDA issued a Cleared decision on October 7, 2005 after a review of 42 days - a notably fast clearance cycle.

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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Jpi America, Inc. devices

FDA 510(k) Submission Details - K052341

510(k) Number K052341 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 26, 2005
Decision Date October 07, 2005
Days to Decision 42 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
65d faster than avg
Panel avg: 107d · This submission: 42d
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 159
Devices cleared under the same product code (IZL) and FDA review panel - the closest regulatory comparables to K052341.
OPDIMA DIGITAL MAMMOGRAPHIC X-RAY SYSTEM
K071015 · Siemens Medical Solutions USA, Inc. · May 2007
PULSERA
K061685 · Philips Medical Systems North America Co. · Sep 2006
MINXRAY, MODEL HF100H+
K052721 · Minxray, Inc. · Oct 2005
SEDECAL MOBILE X-RAY UNITS WITH DIGITAL DETECTOR
K043002 · Sedecal., Sa. · Nov 2004
PRACTIX CONVENIO
K042368 · Philips Medical Systems North America Co. · Oct 2004
GE TETHERED PORTABLE DIGITAL RADIOGRAPHIC DETECTOR
K041922 · General Electric Co. · Jul 2004