Cleared Traditional

MICROVISION FAST DETAIL INTENSIFYING SCREEN (K931283) - FDA 510(k) Clearance

Class I Radiology device.

K931283 · E.I. Dupont DE Nemours & Co., Inc. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 1993
Decision
88d
Days
Class 1
Risk

K931283 is an FDA 510(k) clearance for the MICROVISION FAST DETAIL INTENSIFYING SCREEN. Classified as Screen, Intensifying, Radiographic (product code EAM), Class I - General Controls.

Submitted by E.I. Dupont DE Nemours & Co., Inc. (Wilmington, US). The FDA issued a Cleared decision on June 8, 1993 after a review of 88 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1960 - 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 E.I. Dupont DE Nemours & Co., Inc. devices

Submission Details

510(k) Number K931283 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 12, 1993
Decision Date June 08, 1993
Days to Decision 88 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
19d faster than avg
Panel avg: 107d · This submission: 88d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code EAM Screen, Intensifying, Radiographic
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 892.1960
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.

Regulatory Peers - EAM Screen, Intensifying, Radiographic

All 34
Devices cleared under the same product code (EAM) and FDA review panel - the closest regulatory comparables to K931283.
KODAK INSIGHT TWIN-LOAD INSERT
K942909 · Eastman Kodak Company · Jul 1994
ULTRA-VISION RAPID INTENSIFYING SCREEN
K920190 · E.I. Dupont DE Nemours & Co., Inc. · May 1992
ULTRA-VISION DETAIL INTENSIFYING SCREEN
K920200 · E.I. Dupont DE Nemours & Co., Inc. · May 1992
ULTRA-VISION FAST DETAIL INTENSIFYING SCREEN
K920194 · E.I. Dupont DE Nemours & Co., Inc. · May 1992
CRONEX QUANTA RAPID SR397 RARE EARTH INTENS SCREEN
K900448 · E.I. Dupont DE Nemours & Co., Inc. · Feb 1990
CRONEX QUANTA SR300 INTENSIFYING SCREEN
K900103 · E.I. Dupont DE Nemours & Co., Inc. · Feb 1990