Bio-Scan, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bio-Scan, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Bio-Scan, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1984 to 2001. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Bio-Scan, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bio-Scan, Inc.
6 devices
Cleared
May 11, 2001
BIOFIND
Neurology
183d
Cleared
Dec 03, 1993
EEG ANALYZER
Neurology
385d
Cleared
Mar 31, 1987
BIO-LOG 8+1 AMBULATORY PHYSIOLOGIC RECORDER
Neurology
105d
Cleared
Jun 07, 1984
Q.P. PREAMPLIFIER SYS
Neurology
45d
Cleared
Jun 07, 1984
BIO/SCAN BIOLOG CASSETTE RECORDER
Neurology
45d
Cleared
Jun 07, 1984
EEG ELECTRODES
Neurology
45d