Cleared Traditional

K771718 - CARDIOTHERM-500X

K771718 is the FDA 510(k) clearance for CARDIOTHERM-500X by Columbus Instruments Intl. Corp.. It is a Class 2 Cardiovascular device (product code DXG) cleared through the Traditional 510(k) pathway after a 16-day FDA review.

K771718 · Columbus Instruments Intl. Corp. · Cardiovascular device
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Sep 1977
Decision
16d
Days
Class 2
Risk

K771718 is an FDA 510(k) clearance for the CARDIOTHERM-500X. Classified as Computer, Diagnostic, Pre-programmed, Single-function (product code DXG), Class II - Special Controls.

Submitted by Columbus Instruments Intl. Corp. (Mchenry, US). The FDA issued a Cleared decision on September 28, 1977 after a review of 16 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1435 - 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 Columbus Instruments Intl. Corp. devices

Submission Details

510(k) Number K771718 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 12, 1977
Decision Date September 28, 1977
Days to Decision 16 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
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 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 53
Devices cleared under the same product code (DXG) and FDA review panel - the closest regulatory comparables to K771718.
LVV OPTION
K781855 · Honeywell, Inc. · Jan 1979
LIGHT-PEN SYSTEM FOR QUANTI. ANALY.
K772158 · Varian Assoc., Inc. · Nov 1977
CARDIAC OUTPUT THERMODILUTION MODULE
K771991 · Abbott Laboratories · Nov 1977
CARDIAC CATHETERIZATION LAB MONITOR SYS
K770179 · General Electric Co. · Apr 1977
BATTERY OPERATED FLOW RATE COMPUTER
K760756 · 3M Health Care, Sarns · Oct 1976
TIME-SHARING MULTIPLEXER (MODEL 78308A)
K760774 · Hewlett-Packard Co. · Oct 1976