Cardio Data is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardio Data - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Cardio Data has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1977 to 1985. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardio Data Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardio Data
6 devices
Cleared
Oct 11, 1985
CARDIO DATA PACERECORDER PR3
Cardiovascular
67d
Cleared
Feb 01, 1985
CARDIO DATA MK4 HOLTER ANALYSIS SYSTEM
Cardiovascular
18d
Cleared
Jan 30, 1984
CARDIODATA PACE RECORDER
Cardiovascular
54d
Cleared
May 09, 1983
CARDIO DATA PACEMAKER RECORDER
Cardiovascular
28d
Cleared
Aug 31, 1981
CARDIO-DATA SYSTEM, #MARK III
Cardiovascular
34d
Cleared
Feb 16, 1977
PACEGUARD
Cardiovascular
5d