Cleared Traditional

K952233 - CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628 (FDA 510(k) Clearance)

Class I Radiology device.

K952233 · Victoreen, Inc. · Radiology device
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Jun 1995
Decision
35d
Days
Class 1
Risk

K952233 is an FDA 510(k) clearance for the CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628. Classified as Screen, Leaded, Operator Radiation Protector (product code EAK), Class I - General Controls.

Submitted by Victoreen, Inc. (Cleveland, US). The FDA issued a Cleared decision on June 16, 1995 after a review of 35 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.6500 - 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 Victoreen, Inc. devices

Submission Details

510(k) Number K952233 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 12, 1995
Decision Date June 16, 1995
Days to Decision 35 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
72d faster than avg
Panel avg: 107d · This submission: 35d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code EAK Screen, Leaded, Operator Radiation Protector
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 892.6500
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.