Cleared Traditional

K953832 - SOLARIX FV

K953832 is an FDA 510(k) clearance for SOLARIX FV, manufactured by GE Medical Systems. The device is a Class 2 Radiology device with product code KPR cleared through the Traditional 510(k) pathway after a 27-day FDA review.

K953832 · GE Medical Systems · Radiology device
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Sep 1995
Decision
27d
Days
Class 2
Risk

K953832 is an FDA 510(k) clearance for the SOLARIX FV. Classified as System, X-ray, Stationary (product code KPR), Class II - Special Controls.

Submitted by GE Medical Systems (Milwaukee, US). The FDA issued a Cleared decision on September 12, 1995 after a review of 27 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 GE Medical Systems devices

FDA 510(k) Submission Details - K953832

510(k) Number K953832 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 16, 1995
Decision Date September 12, 1995
Days to Decision 27 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
80d faster than avg
Panel avg: 107d · This submission: 27d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KPR Device Classification - Class 2, Special Controls

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.

Regulatory Peers - KPR System, X-ray, Stationary

All 192
Devices cleared under the same product code (KPR) and FDA review panel - the closest regulatory comparables to K953832.
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K954196 · Philips Medical Systems (Cleveland), Inc. · Oct 1995
VERTICAL INTEGRATED PERFECT VIEW (VIP) RADIOGRAPHIC SYSTEM
K952672 · Bennett X-Ray Corp. · Jul 1995
PHILIPS BUCKY DIAGNOST FAMILY
K945278 · Philips Medical Systems North America, Inc. · Dec 1994
PHILIPS THORAVISION
K931071 · Philips Medical Systems, Inc. · Sep 1994