Visicu, Inc. is one of 16294 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Visicu, Inc. - FDA 510(k) Cleared Devices
Recent clearances: eCareManager 4.5, eCareManager 4.1, eCareCoordinator
7
Total
7
Cleared
0
Denied
Visicu, Inc. has 7 FDA 510(k) cleared medical devices. Based in Lake Forest, US.
Last cleared in 2022. Active since 2000. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Visicu, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Visicu, Inc.
7 devices
Cleared
Jun 03, 2022
eCareManager 4.5
Cardiovascular
421d
Cleared
Aug 03, 2017
eCareManager 4.1
Cardiovascular
90d
Cleared
Jul 14, 2017
eCareCoordinator
Cardiovascular
99d
Cleared
Sep 30, 2016
eCareManager 4.0.1
Cardiovascular
333d
Cleared
Sep 09, 2014
ECARE COORDINATOR (ECC)
Cardiovascular
77d
Cleared
Jul 24, 2001
MODIFICATION TO: ARGUS SYSTEM-CONTINUOUS EXPERT CARE NETWORK W/SMART ALRAMS
Cardiovascular
12d
Cleared
Oct 27, 2000
ARGUS SYSTEM-CONTINUOUS EXPERT CARE NETWORK
Cardiovascular
121d