Non-Invasive Monitoring Systems, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Non-Invasive Monitoring Systems, Inc. has 6 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 6 cleared submissions from 1989 to 2001. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Non-Invasive Monitoring Systems, Inc. Filter by specialty or product code using the sidebar.
6 devices
Cleared
Aug 21, 2001
RESPIEVENTS SOFTWARE IS EVENT DATA PROCESSING SOFWARE FOR A PC
Cardiovascular
54d
Cleared
Jul 26, 2000
RESPIEVENTS, VERSION 4.2
Cardiovascular
86d
Cleared
Feb 13, 1996
RESPIEVENTS
Cardiovascular
610d
Cleared
Feb 13, 1996
RESPITRACE PT
Cardiovascular
610d
Cleared
Mar 29, 1991
RESPITRACE PLUS, RESPIBANDS, AND RESPICENTRAL
Anesthesiology
263d
Cleared
Jun 08, 1989
RESPITRAK
Anesthesiology
191d