Cleared Traditional

K811792 - ARRYTHMIA PRINTER OPTION

K811792 is the FDA 510(k) clearance for ARRYTHMIA PRINTER OPTION by American Edwards Laboratories. It is a Class 2 Cardiovascular device (product code DSI) cleared through the Traditional 510(k) pathway after a 16-day FDA review.

K811792 · American Edwards Laboratories · Cardiovascular device
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Jul 1981
Decision
16d
Days
Class 2
Risk

K811792 is an FDA 510(k) clearance for the ARRYTHMIA PRINTER OPTION. Classified as Detector And Alarm, Arrhythmia (product code DSI), Class II - Special Controls.

Submitted by American Edwards Laboratories (Mchenry, US). The FDA issued a Cleared decision on July 10, 1981 after a review of 16 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1025 - 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 American Edwards Laboratories devices

Submission Details

510(k) Number K811792 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 24, 1981
Decision Date July 10, 1981
Days to Decision 16 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
109d faster than avg
Panel avg: 125d · This submission: 16d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DSI Detector And Alarm, Arrhythmia
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1025
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 - DSI Detector And Alarm, Arrhythmia

All 218
Devices cleared under the same product code (DSI) and FDA review panel - the closest regulatory comparables to K811792.
MICRO-PREPROCESSOR UNIT
K812914 · General Electric Co. · Dec 1981
ARRHYTHMIA FUNCTION BLOCK
K811581 · Honeywell, Inc. · Aug 1981
THE BETA
K810940 · Burdick Corp. · Jul 1981
DEL MAR AVIONICS MODELS 9400 & 9401
K811122 · Del Mar Avionics · Jun 1981
SIRECUST 358
K803208 · Siemens Corp. · May 1981
GUARDIAN MONITOR (CARDIOVASCULAR)
K803282 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Feb 1981