Cleared Traditional

K871282 - SYNECTICS LIBERTY SYSTEM AMPLIFIER AND SOFTWARE (FDA 510(k) Clearance)

Class I Gastroenterology & Urology device.

K871282 · Synectics-Dantec · Gastroenterology & Urology device
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Jun 1987
Decision
71d
Days
Class 1
Risk

K871282 is an FDA 510(k) clearance for the SYNECTICS LIBERTY SYSTEM AMPLIFIER AND SOFTWARE. Classified as Electrode, Ph, Stomach (product code FFT), Class I - General Controls.

Submitted by Synectics-Dantec (Milwaukee, US). The FDA issued a Cleared decision on June 10, 1987 after a review of 71 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1400 - the FDA gastroenterology and urology 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 Synectics-Dantec devices

Submission Details

510(k) Number K871282 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 31, 1987
Decision Date June 10, 1987
Days to Decision 71 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
59d faster than avg
Panel avg: 130d · This submission: 71d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code FFT Electrode, Ph, Stomach
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 876.1400
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.