Cleared Traditional

DDRCOMPACT, DDRCOMPACT PLUS AND DDRCOMPACT CHEST (K070678) - FDA 510(k) Clearance

Class II Radiology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K070678 · Swissray International, Inc. · Radiology device
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May 2007
Decision
51d
Days
Class 2
Risk

K070678 is an FDA 510(k) clearance for the DDRCOMPACT, DDRCOMPACT PLUS AND DDRCOMPACT CHEST. Classified as System, X-ray, Stationary (product code KPR), Class II - Special Controls.

Submitted by Swissray International, Inc. (Elizabeth, US). The FDA issued a Cleared decision on May 2, 2007 after a review of 51 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1680 - 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 Swissray International, Inc. devices

Submission Details

510(k) Number K070678 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 12, 2007
Decision Date May 02, 2007
Days to Decision 51 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
56d faster than avg
Panel avg: 107d · This submission: 51d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KPR System, X-ray, Stationary
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1680
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.

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