Cardiac Output Computer

FDA 510(k) K760600 · Cardiopulmonary Instrumentation

Substantially Equivalent

510(k) numberK760600

Submission

Device name
Cardiac Output Computer
Applicant
Cardiopulmonary Instrumentation
Mchenry, IL, US
Received
September 7, 1976
Decision date
October 15, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DXG – Computer, Diagnostic, Pre-Programmed, Single-Function
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1435
Specialty
Cardiovascular

Other 510(k)s with product code DXG

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K232048Cogent™ Hemodynamic Monitoring System; Cogent™ HMSDXG · Traditional Icu Medical12/20/2023SE
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K193179EV1000 Clinical PlatformDXG · Special Edwards Lifesciences, LLC12/17/2019SE
K190955Hypotension Decision AssistDXG · Traditional Directed Systems, Ltd.11/27/2019SE
K181372ArgosDXG · Traditional Retia Medical, LLC12/13/2018SE
K172259PulsioFlex Monitoring SystemDXG · Traditional Pulsion Medical Systems SE01/18/2018SE
K163334LiDCOunity v2 Hemodynamic MonitorDXG · Traditional Lidco, Ltd.06/05/2017SE

Questions and answers

When was Cardiac Output Computer cleared by the FDA?

Cardiac Output Computer (K760600) received a 510(k) decision of Substantially Equivalent on October 15, 1976, 38 days after the submission was received.

What is the product code of K760600?

The FDA product code is DXG – Computer, Diagnostic, Pre-Programmed, Single-Function, a Class II (moderate risk) device regulated under 21 CFR 870.1435.