Cleared Traditional

K952672 - VERTICAL INTEGRATED PERFECT VIEW (VIP) ...

K952672 is an FDA 510(k) clearance for VERTICAL INTEGRATED PERFECT VIEW (VIP) ..., manufactured by Bennett X-Ray Corp.. The device is a Class 2 Radiology device with product code KPR cleared through the Traditional 510(k) pathway after a 31-day FDA review.

K952672 · Bennett X-Ray Corp. · Radiology device
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Jul 1995
Decision
31d
Days
Class 2
Risk

K952672 is an FDA 510(k) clearance for the VERTICAL INTEGRATED PERFECT VIEW (VIP) RADIOGRAPHIC SYSTEM. Classified as System, X-ray, Stationary (product code KPR), Class II - Special Controls.

Submitted by Bennett X-Ray Corp. (Copiague, US). The FDA issued a Cleared decision on July 13, 1995 after a review of 31 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 Bennett X-Ray Corp. devices

FDA 510(k) Submission Details - K952672

510(k) Number K952672 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 12, 1995
Decision Date July 13, 1995
Days to Decision 31 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
76d faster than avg
Panel avg: 107d · This submission: 31d
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 191
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