Cleared Traditional

K870030 - THE SCREENER GSI 55 ABR SCREENER

K870030 is an FDA 510(k) clearance for THE SCREENER GSI 55 ABR SCREENER, manufactured by Grason-Stadler, Inc.. The device is a Class 2 Neurology device with product code GWJ cleared through the Traditional 510(k) pathway after a 67-day FDA review.

K870030 · Grason-Stadler, Inc. · Neurology device
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Mar 1987
Decision
67d
Days
Class 2
Risk

K870030 is an FDA 510(k) clearance for the THE SCREENER GSI 55 ABR SCREENER. Classified as Stimulator, Auditory, Evoked Response (product code GWJ), Class II - Special Controls.

Submitted by Grason-Stadler, Inc. (Littleton, US). The FDA issued a Cleared decision on March 13, 1987 after a review of 67 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.1900 - the FDA neurology device 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 Grason-Stadler, Inc. devices

FDA 510(k) Submission Details - K870030

510(k) Number K870030 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 05, 1987
Decision Date March 13, 1987
Days to Decision 67 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
81d faster than avg
Panel avg: 148d · This submission: 67d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GWJ Device Classification - Class 2, Special Controls

Product Code GWJ Stimulator, Auditory, Evoked Response
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.1900
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 Neurology devices follow this clearance model.

Regulatory Peers - GWJ Stimulator, Auditory, Evoked Response

All 22
Devices cleared under the same product code (GWJ) and FDA review panel - the closest regulatory comparables to K870030.
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K863985 · Jedmed Instrument Co. · Jan 1987