Cleared Traditional

K833000 - I-CHANNEL RECORDER (FDA 510(k) Clearance)

Class I Cardiovascular device.

K833000 · Litton Medical Electronics · Cardiovascular device
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Jun 1984
Decision
288d
Days
Class 1
Risk

K833000 is an FDA 510(k) clearance for the I-CHANNEL RECORDER. Classified as Recorder, Paper Chart (product code DSF), Class I - General Controls.

Submitted by Litton Medical Electronics (Walker, US). The FDA issued a Cleared decision on June 1, 1984 after a review of 288 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2810 - the FDA cardiovascular device 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

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Submission Details

510(k) Number K833000 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 18, 1983
Decision Date June 01, 1984
Days to Decision 288 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
163d slower than avg
Panel avg: 125d · This submission: 288d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code DSF Recorder, Paper Chart
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 870.2810
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.