Cambridge Heart CH 2000 Stress Test System

FDA 510(k) K950018 · Cambridge Heart, Inc.

Substantially Equivalent

510(k) numberK950018

Submission

Device name
Cambridge Heart CH 2000 Stress Test System
Applicant
Cambridge Heart, Inc.
Bedford, MA, US
Received
January 3, 1995
Decision date
February 29, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
DPS – Electrocardiograph
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2340
Specialty
Cardiovascular

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K243305Masimo W1DPS · Traditional Masimo Corporation04/03/2025SE
K241217CloudHRV™ System (100-01-001)DPS · Traditional Inmedix, Inc.01/16/2025SE
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More from Masimo Corporation

510(k)DeviceDecision
K100362Cambridge Heart OemDQK · Special 04/14/2010SE
K050225Heartwave II Cardiac Diagnostic SystemDQK · Special 04/07/2005SE
K022152Heartwave Alternans Processing System, Model ApsDPS · Special 07/16/2002SE
K022149Cardiac Diagnostic System, Model CH2000DPS · Special 07/16/2002SE
K013565Cardiac Diagnostic System, Model CH2000DPS · Special 11/21/2001SE
K013564Modification to Heartwave Alternans Processing System, Model ApsDPS · Special 11/21/2001SE
K012206Alternanas Processing System, CH 2000 Cardiac Diagnostic System, Heartwave Alternans…DQK · Traditional 10/12/2001SE
K011324Cambridge Heart Model CH 2000 Cardiac Diagnostic SystemDQK · Special 05/23/2001SE
K010758Heartwave Alternans Processing System, ApsDPS · Special 04/12/2001SE
K010756CH 2000 Cardiac Diagnostic SystemDQK · Special 04/12/2001SE

Questions and answers

When was Cambridge Heart CH 2000 Stress Test System cleared by the FDA?

Cambridge Heart CH 2000 Stress Test System (K950018) received a 510(k) decision of Substantially Equivalent on February 29, 1996, 422 days after the submission was received.

What is the product code of K950018?

The FDA product code is DPS – Electrocardiograph, a Class II (moderate risk) device regulated under 21 CFR 870.2340.