Cleared Traditional

K951765 - SERIES 6600 DIGITAL MOBILE C-ARM

K951765 is an FDA 510(k) clearance for SERIES 6600 DIGITAL MOBILE C-ARM, manufactured by Ge Dec Medical Systems. The device is a Class 2 Radiology device with product code OXO cleared through the Traditional 510(k) pathway after a 24-day FDA review.

K951765 · Ge Dec Medical Systems · Radiology device
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May 1995
Decision
24d
Days
Class 2
Risk

K951765 is an FDA 510(k) clearance for the SERIES 6600 DIGITAL MOBILE C-ARM. Classified as Image-intensified Fluoroscopic X-ray System, Mobile (product code OXO), Class II - Special Controls.

Submitted by Ge Dec Medical Systems (Salt Lake City, US). The FDA issued a Cleared decision on May 11, 1995 after a review of 24 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 Ge Dec Medical Systems devices

FDA 510(k) Submission Details - K951765

510(k) Number K951765 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 17, 1995
Decision Date May 11, 1995
Days to Decision 24 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
83d faster than avg
Panel avg: 107d · This submission: 24d
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 41
Devices cleared under the same product code (OXO) and FDA review panel - the closest regulatory comparables to K951765.
SIREMOBIL COMPACT
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SHIMADZU MOBILE X-RAY SYSTEMS
K940294 · Shimadzu Precision Instruments, Inc. · Mar 1994
STENOSCOP MOBILE FLUOROSCOPIC XRAY SYSTEM
K933447 · GE Medical Systems · Aug 1993
COMET C-125
K914748 · Fischer Imaging Corp. · Oct 1992