Biosensor Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biosensor Corp. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Biosensor Corp. has 10 FDA 510(k) cleared cardiovascular devices. Based in Walker, US.
Historical record: 10 cleared submissions from 1983 to 1999.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biosensor Corp.
10 devices
Cleared
Jun 14, 1999
BIOSENSOR HOLTER MONITOR SYSTEM SOFTWARE, MODEL 1005
Cardiovascular
84d
Cleared
Mar 04, 1998
BIOSENSOR HOLTER MONITOR SYSTEM
Cardiovascular
117d
Cleared
Mar 04, 1998
BIOSENSOR HOLTER MONITOR SYSTEM
Cardiovascular
90d
Cleared
Jun 18, 1996
AMBULATORY (HOLTER) RECORDING SYSTEM
Cardiovascular
487d
Cleared
May 30, 1996
PC ECG 1200 ECG AND STRESS ELECTROCARDIOGRAPHY TESTING SYSTEM(VERSION 2.90)
Cardiovascular
121d
Cleared
Apr 12, 1996
BIOSENSOR BIDOP VASCULAR TEST SYSTEM
Radiology
640d
Cleared
Feb 09, 1996
AMBULATORY (HOLTER) RECORDING SYSTEM
Cardiovascular
358d
Cleared
Feb 17, 1993
AMBULATORY (HOLTER) RECORDING, MODIFICATION
Cardiovascular
328d
Cleared
Jan 26, 1990
AMBULATORY (HOLTER) RECORDING SYSTEM - MODIFIED
Cardiovascular
156d
Cleared
Dec 01, 1983
BIOSENSOR ASC SYSTEM
Cardiovascular
192d