Cleared Traditional

K082167 - PORTABLE X-RAY SYSTEM, MODELS DIOX-602, PROX

K082167 is an FDA 510(k) clearance for PORTABLE X-RAY SYSTEM, manufactured by Digimed Corporation. The device is a Class 2 Radiology device with product code EHD cleared through the Traditional 510(k) pathway after a 57-day FDA review.

K082167 · Digimed Corporation · Radiology device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Sep 2008
Decision
57d
Days
Class 2
Risk

K082167 is an FDA 510(k) clearance for the PORTABLE X-RAY SYSTEM, MODELS DIOX-602, PROX. Classified as Unit, X-ray, Extraoral With Timer (product code EHD), Class II - Special Controls.

Submitted by Digimed Corporation (Salt Lake City, US). The FDA issued a Cleared decision on September 26, 2008 after a review of 57 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 872.1800 - 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 - K082167

510(k) Number K082167 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 31, 2008
Decision Date September 26, 2008
Days to Decision 57 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
50d faster than avg
Panel avg: 107d · This submission: 57d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EHD Device Classification - Class 2, Special Controls

Product Code EHD Unit, X-ray, Extraoral With Timer
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.1800
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 - EHD Unit, X-ray, Extraoral With Timer

All 177
Devices cleared under the same product code (EHD) and FDA review panel - the closest regulatory comparables to K082167.
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K082167 · PORTABLE X-RAY SYSTEM, MODELS DIOX-602, PROX
Download PDF FDA Summary Digimed Corporation