Cleared Traditional

DMI SERIES 90 EXAMINATION TABLE (K894788) - FDA 510(k) Clearance

Class I General Hospital device.

K894788 · M.D. Intl., Inc. · General Hospital
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Sep 1989
Decision
42d
Days
Class 1
Risk

K894788 is an FDA 510(k) clearance for the DMI SERIES 90 EXAMINATION TABLE. Classified as Chair And Table, Medical (product code KMN), Class I - General Controls.

Submitted by M.D. Intl., Inc. (Salt Lake City, US). The FDA issued a Cleared decision on September 8, 1989 after a review of 42 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6140 - the FDA general hospital 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 M.D. Intl., Inc. devices

Submission Details

510(k) Number K894788 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 28, 1989
Decision Date September 08, 1989
Days to Decision 42 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
87d faster than avg
Panel avg: 129d · This submission: 42d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KMN Chair And Table, Medical
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6140
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.