Cleared Traditional

K961826 - DIGIPAN

K961826 is an FDA 510(k) clearance for DIGIPAN, manufactured by Trophy Radiologie. The device is a Class 2 Radiology device with product code EHD cleared through the Traditional 510(k) pathway after a 133-day FDA review.

K961826 · Trophy Radiologie · Radiology device
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Sep 1996
Decision
133d
Days
Class 2
Risk

K961826 is an FDA 510(k) clearance for the DIGIPAN. Classified as Unit, X-ray, Extraoral With Timer (product code EHD), Class II - Special Controls.

Submitted by Trophy Radiologie (Vincennes, Cedex (Paris), FR). The FDA issued a Cleared decision on September 23, 1996 after a review of 133 days - within the typical 510(k) review window.

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: 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 Trophy Radiologie devices

FDA 510(k) Submission Details - K961826

510(k) Number K961826 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 13, 1996
Decision Date September 23, 1996
Days to Decision 133 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
26d slower than avg
Panel avg: 107d · This submission: 133d
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 94
Devices cleared under the same product code (EHD) and FDA review panel - the closest regulatory comparables to K961826.
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K970263 · Planmeca Oy · Feb 1997
ORTHORALIX E/GX-9000 PANORAMIC X-RAY SYSTEM
K964659 · Dentsply Intl. · Dec 1996
TOMOGRAPH ACCESSORIES
K962120 · Steri-Oss, Inc. · Jul 1996
ELITYS OR ELITYS-E
K962337 · Trophy Radiologie · Jul 1996
PROSTYLE INTRA
K955429 · Planmeca Oy · Dec 1995