Cambridge Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cambridge Instruments, Inc. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Cambridge Instruments, Inc. has 13 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 13 cleared submissions from 1976 to 1981.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cambridge Instruments, Inc.
13 devices
Cleared
Jun 30, 1981
CENTRAL STATION MONITORING SYSTEMS
Cardiovascular
67d
Cleared
May 29, 1981
CAMPBRIDGE COMPUTRACE
Cardiovascular
42d
Cleared
Jan 13, 1981
4-CHANNEL ECG TELEMETRY MON. SYST. #3045
Cardiovascular
25d
Cleared
Jun 26, 1980
CAMBRIDGE CARDIAC DIAGNOSTIC SYSTEM
Cardiovascular
35d
Cleared
Apr 08, 1980
CAMBRIDGE VS-550 ELECTROCARDIOGRAPH
Cardiovascular
26d
Cleared
Feb 19, 1980
TREADMILL MODEL 3060
Physical Medicine
55d
Cleared
Sep 17, 1979
SCINTISTRESS SYSTEM
Cardiovascular
81d
Cleared
Mar 23, 1979
CARDIOCASSETTE II, AMBULATORY ECG SYSTEM
Cardiovascular
8d
Cleared
Jan 06, 1977
3038 OPTION B-COMPUT. TRANS. TERMINAL
Cardiovascular
10d
Cleared
Dec 09, 1976
MODEL 3044 3-CHANNEL STRESS TEST SYSTEM
Cardiovascular
3d
Cleared
Nov 09, 1976
ELECTROCARDIOGRAPH (MODEL VS-4B)
Cardiovascular
11d
Cleared
Oct 08, 1976
IMPEDANCE TESTER (MODEL 4370)
Cardiovascular
4d
Cleared
Oct 08, 1976
IMPEDANCE TESTER (MODEL 4390)
Cardiovascular
4d