Cleared Traditional

K122697 - PORTA 100HF

K122697 is an FDA 510(k) clearance for PORTA 100HF, manufactured by Job Corporation. The device is a Class 2 Radiology device with product code IZL cleared through the Traditional 510(k) pathway after a 31-day FDA review.

K122697 · Job Corporation · Radiology device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Oct 2012
Decision
31d
Days
Class 2
Risk

K122697 is an FDA 510(k) clearance for the PORTA 100HF. Classified as System, X-ray, Mobile (product code IZL), Class II - Special Controls.

Submitted by Job Corporation (Gardena, US). The FDA issued a Cleared decision on October 5, 2012 after a review of 31 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.

FDA 510(k) Submission Details - K122697

510(k) Number K122697 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 04, 2012
Decision Date October 05, 2012
Days to Decision 31 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
76d faster than avg
Panel avg: 107d · This submission: 31d
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 219
Devices cleared under the same product code (IZL) and FDA review panel - the closest regulatory comparables to K122697.
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K122697 · PORTA 100HF
Download PDF FDA Summary Job Corporation