Cambridge Heart, Inc.
Cambridge Heart, Inc. holds FDA 510(k) medical device clearances, first cleared 1996, most recent 2010.
Top product codes for Cambridge Heart, Inc.
Recent clearances by Cambridge Heart, Inc.
- K100362 — CAMBRIDGE HEART OEM
- K050225 — HEARTWAVE II CARDIAC DIAGNOSTIC SYSTEM
- K022149 — CARDIAC DIAGNOSTIC SYSTEM, MODEL CH2000
- K022152 — HEARTWAVE ALTERNANS PROCESSING SYSTEM, MODEL APS
- K013564 — MODIFICATION TO HEARTWAVE ALTERNANS PROCESSING SYSTEM, MODEL APS
- K013565 — CARDIAC DIAGNOSTIC SYSTEM, MODEL CH2000
- K012206 — ALTERNANAS PROCESSING SYSTEM, CH 2000 CARDIAC DIAGNOSTIC SYSTEM, HEARTWAVE ALTERNANS PROCESSING SYSTEM
- K011324 — CAMBRIDGE HEART MODEL CH 2000 CARDIAC DIAGNOSTIC SYSTEM
- K010756 — CH 2000 CARDIAC DIAGNOSTIC SYSTEM
- K010758 — HEARTWAVE ALTERNANS PROCESSING SYSTEM, APS
- K003492 — ANALYTIC SPECTRAL METHOD OF ALTERNANS PROCESSING; CH 2000 CARDIAC DIAGNOSTIC SYSTEM; HEARTWAVE ALTERNANS PROCESSING SYS
- K002230 — CAMBRIDGE HEART MICRO-V ALTERNANS SENSOR, MODEL 20327-002
- K001034 — MODEL APS ALTERNANS PROCESSING SYSTEM
- K983102 — CARDIAC DIAGNOSTIC SYSTEM MODEL CH 2000
- K981697 — CAMBRIDGE HEART CH 2000 CARDIAC DIAGNOSTIC SYSTEM
- K962115 — CAMBRIDGE HEART HI-RES ECG ELECTRODE
- K950018 — CAMBRIDGE HEART CH 2000 STRESS TEST SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.