Cambridge Medical Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cambridge Medical Instruments, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Cambridge Medical Instruments, Inc. has 8 FDA 510(k) cleared medical devices. Based in Ossining, US.
Historical record: 8 cleared submissions from 1985 to 1990. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cambridge Medical Instruments, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cambridge Medical Instruments, Inc.
8 devices
Cleared
Feb 26, 1990
EKG, ECG KENZ, ECG 302
Cardiovascular
87d
Cleared
Feb 26, 1990
EKG, ECG KENZ, ECG 303
Cardiovascular
87d
Cleared
Jan 04, 1990
MODEL MC6500 ELECTROCARDIOGRAPH
Cardiovascular
86d
Cleared
Jan 25, 1989
MC6700 MULTI-CHANNEL ELECTROCARDIOGRAPH
Cardiovascular
163d
Cleared
Nov 23, 1987
MC 6000 MULTI-CHANNEL ELECTROCARDIOGRAPH
Cardiovascular
181d
Cleared
Aug 25, 1986
MODEL SC-1000 ELECTROCARDIOGRAPH SPECIFICATION
Cardiovascular
35d
Cleared
Jan 08, 1986
PREVIEW XT
Cardiovascular
76d
Cleared
Nov 13, 1985
CAMBRIDGE MODEL XT1000
Physical Medicine
20d