Calnor of EL Paseo, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Calnor of EL Paseo, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Calnor of EL Paseo, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1977 to 1984. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Calnor of EL Paseo, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Calnor of EL Paseo, Inc.
6 devices
Cleared
Jul 17, 1984
GSR, 126, EEG 130-TEMP. 132, EMG 133
Neurology
71d
Cleared
Jul 17, 1984
EEG 130
Neurology
71d
Cleared
Jul 17, 1984
TEMPERATURE 132
Neurology
71d
Cleared
Jul 17, 1984
EMG MODEL 133
Neurology
71d
Cleared
Mar 19, 1984
ETHYLENE OXIDE DETECTOR GLD-1-07
General Hospital
109d
Cleared
Aug 26, 1977
CLINICAL EMG MODEL 133
Neurology
8d