Cleared Traditional

K061173 - CPIVISION DIGITAL IMAGING SYSTEM

K061173 is an FDA 510(k) clearance for CPIVISION DIGITAL IMAGING SYSTEM, manufactured by Communications & Power Industries Canada, Inc.. The device is a Class 2 Radiology device with product code OWB cleared through the Traditional 510(k) pathway after a 43-day FDA review.

K061173 · Communications & Power Industries Canada, Inc. · Radiology device
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Jun 2006
Decision
43d
Days
Class 2
Risk

K061173 is an FDA 510(k) clearance for the CPIVISION DIGITAL IMAGING SYSTEM. Classified as Interventional Fluoroscopic X-ray System (product code OWB), Class II - Special Controls.

Submitted by Communications & Power Industries Canada, Inc. (Georgetown, CA). The FDA issued a Cleared decision on June 9, 2006 after a review of 43 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1650 - 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 Communications & Power Industries Canada, Inc. devices

FDA 510(k) Submission Details - K061173

510(k) Number K061173 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 27, 2006
Decision Date June 09, 2006
Days to Decision 43 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
64d faster than avg
Panel avg: 107d · This submission: 43d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

OWB Device Classification - Class 2, Special Controls

Product Code OWB Interventional Fluoroscopic X-ray System
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1650
Definition Interventional Fluoroscopy
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 - OWB Interventional Fluoroscopic X-ray System

All 248
Devices cleared under the same product code (OWB) and FDA review panel - the closest regulatory comparables to K061173.
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