Cleared Traditional

K791151 - ECG CHANNEL OF DIAGNOSTIC SYSTEM

K791151 is an FDA 510(k) clearance for ECG CHANNEL OF DIAGNOSTIC SYSTEM, manufactured by Honeywell, Inc.. The device is a Class 2 Cardiovascular device with product code DPS cleared through the Traditional 510(k) pathway after a 40-day FDA review.

K791151 · Honeywell, Inc. · Cardiovascular device
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Jul 1979
Decision
40d
Days
Class 2
Risk

K791151 is an FDA 510(k) clearance for the ECG CHANNEL OF DIAGNOSTIC SYSTEM. Classified as Electrocardiograph (product code DPS), Class II - Special Controls.

Submitted by Honeywell, Inc. (Mchenry, US). The FDA issued a Cleared decision on July 30, 1979 after a review of 40 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2340 - 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 Honeywell, Inc. devices

FDA 510(k) Submission Details - K791151

510(k) Number K791151 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 20, 1979
Decision Date July 30, 1979
Days to Decision 40 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
85d faster than avg
Panel avg: 125d · This submission: 40d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DPS Device Classification - Class 2, Special Controls

Product Code DPS Electrocardiograph
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2340
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 - DPS Electrocardiograph

All 275
Devices cleared under the same product code (DPS) and FDA review panel - the closest regulatory comparables to K791151.
MODEL 685/686 DYNAMIC ELECTROCARDI0-
K792072 · Del Mar Avionics · Nov 1979
ELECTROCARDIOGRAPH MODEL ECG-5403
K791540 · Nihon Kohden America, Inc. · Sep 1979
QUINTON MODEL 630 AND 636 ECG DATA CART
K791364 · Quinton, Inc. · Aug 1979
MODEL 78501A PATIENT MONITORING SYSTEM
K790939 · Hewlett-Packard Co. · Jun 1979
QUINTON MODEL 530X ECG DATA CART
K790739 · Quinton, Inc. · Apr 1979
ELECTROCARDIOGRAPH, EK-9
K790114 · Burdick Corp. · Feb 1979