Cleared Traditional

K792080 - MODEL 656 ARRHYTHMIA ANALYZER

K792080 is the FDA 510(k) clearance for MODEL 656 ARRHYTHMIA ANALYZER by Del Mar Avionics. It is a Class 2 Cardiovascular device (product code DXG) cleared through the Traditional 510(k) pathway after a 50-day FDA review.

K792080 · Del Mar Avionics · Cardiovascular device
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Dec 1979
Decision
50d
Days
Class 2
Risk

K792080 is an FDA 510(k) clearance for the MODEL 656 ARRHYTHMIA ANALYZER. Classified as Computer, Diagnostic, Pre-programmed, Single-function (product code DXG), Class II - Special Controls.

Submitted by Del Mar Avionics (Mchenry, US). The FDA issued a Cleared decision on December 4, 1979 after a review of 50 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1435 - 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: 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 Del Mar Avionics devices

Submission Details

510(k) Number K792080 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 15, 1979
Decision Date December 04, 1979
Days to Decision 50 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
75d faster than avg
Panel avg: 125d · This submission: 50d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DXG Computer, Diagnostic, Pre-programmed, Single-function
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1435
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 Cardiovascular devices follow this clearance model.

Regulatory Peers - DXG Computer, Diagnostic, Pre-programmed, Single-function

All 79
Devices cleared under the same product code (DXG) and FDA review panel - the closest regulatory comparables to K792080.
PDS THERMAL DILUTION CARDIAC MODULE(OUT)
K802316 · General Electric Co. · Nov 1980
MLC-4200 CARDIAC OUTPUT COMPUTER
K802305 · Nihon Kohden America, Inc. · Oct 1980
CARDIAC OUTPUT COMPUTER, M-MLC-4100
K792678 · Nihon Kohden America, Inc. · Jan 1980
STORAGE, DIGITAL DSC-1, CONTROL UNIT
K790288 · Oxford Medilog, Inc. · Feb 1979
LVV OPTION
K781855 · Honeywell, Inc. · Jan 1979
CENTRAL MONITORING SYSTEM
K772152 · Burdick Corp. · Nov 1977