Pulse Time Products, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pulse Time Products, Ltd. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Pulse Time Products, Ltd. has 6 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 6 cleared submissions from 1981 to 1990. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Pulse Time Products, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pulse Time Products, Ltd.
6 devices
Cleared
Aug 23, 1990
BP50 BLOOD PRESSURE AND PULSE MONITOR
Cardiovascular
150d
Cleared
Aug 25, 1989
PULSE TIME PRODUCTS LIMITED, PM-2
Cardiovascular
130d
Cleared
Aug 25, 1989
PULSE TIME PRODUCTS LIMITED, PM-3
Cardiovascular
130d
Cleared
Jun 24, 1987
PULSE/B.P. MONITOR
Cardiovascular
229d
Cleared
Mar 20, 1987
PM-8 HEART RATE MONITOR
Cardiovascular
105d
Cleared
Sep 16, 1981
CARDIACMONITORS
Cardiovascular
117d