Cleared Traditional

K003837 - FLEXIVIEW 8800 DIGITAL MOBILE IMAGING SYSTEM

K003837 is an FDA 510(k) clearance for FLEXIVIEW 8800 DIGITAL MOBILE IMAGING S..., manufactured by Ge Oec Medical Systems. The device is a Class 2 Radiology device with product code OXO cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K003837 · Ge Oec Medical Systems · Radiology device
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Mar 2001
Decision
90d
Days
Class 2
Risk

K003837 is an FDA 510(k) clearance for the FLEXIVIEW 8800 DIGITAL MOBILE IMAGING SYSTEM. Classified as Image-intensified Fluoroscopic X-ray System, Mobile (product code OXO), Class II - Special Controls.

Submitted by Ge Oec Medical Systems (Salt Lake City, US). The FDA issued a Cleared decision on March 12, 2001 after a review of 90 days - within the typical 510(k) review window.

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: 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 Ge Oec Medical Systems devices

FDA 510(k) Submission Details - K003837

510(k) Number K003837 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 12, 2000
Decision Date March 12, 2001
Days to Decision 90 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
17d faster than avg
Panel avg: 107d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

OXO Device Classification - Class 2, Special Controls

Product Code OXO Image-intensified Fluoroscopic X-ray System, Mobile
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1650
Definition Fluoroscopy Of The Human Body.
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 - OXO Image-intensified Fluoroscopic X-ray System, Mobile

All 44
Devices cleared under the same product code (OXO) and FDA review panel - the closest regulatory comparables to K003837.
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