Cleared Traditional

K820438 - QUINTON Q2000 ETT MONITORING SYSTEM

K820438 is the FDA 510(k) clearance for QUINTON Q2000 ETT MONITORING SYSTEM by Quinton, Inc.. It is a Class 2 Cardiovascular device (product code DSI) cleared through the Traditional 510(k) pathway after a 71-day FDA review.

K820438 · Quinton, Inc. · Cardiovascular device
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Apr 1982
Decision
71d
Days
Class 2
Risk

K820438 is an FDA 510(k) clearance for the QUINTON Q2000 ETT MONITORING SYSTEM. Classified as Detector And Alarm, Arrhythmia (product code DSI), Class II - Special Controls.

Submitted by Quinton, Inc. (Mchenry, US). The FDA issued a Cleared decision on April 29, 1982 after a review of 71 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 Quinton, Inc. devices

Submission Details

510(k) Number K820438 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 17, 1982
Decision Date April 29, 1982
Days to Decision 71 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
54d faster than avg
Panel avg: 125d · This submission: 71d
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 231
Devices cleared under the same product code (DSI) and FDA review panel - the closest regulatory comparables to K820438.
SERIES 7000 BEDSIDE PATIENT MONITOR
K822718 · Marquette Electronics, Inc. · Oct 1982
MULTIPLE LEAD ARRHYTHMIA MODULE
K822030 · Marquette Electronics, Inc. · Sep 1982
MEMOPORT C
K820881 · Litton Medical Electronics · May 1982
ALGORITHM OF THE ARRHYTHMIA MON. SYS
K820477 · Hewlett-Packard Co. · Apr 1982
MICRO-PREPROCESSOR UNIT
K812914 · General Electric Co. · Dec 1981
ARRHYTHMIA FUNCTION BLOCK
K811581 · Honeywell, Inc. · Aug 1981