Webster Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Webster Laboratories, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Webster Laboratories, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1981 to 1985. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Webster Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Webster Laboratories, Inc.
5 devices
Cleared
Dec 03, 1985
CARDIOVASCULAR, THERMODILUTION, FLOW, CORONARY SIN
Cardiovascular
113d
Cleared
Oct 18, 1984
ELECTRODE CATHETER, ORTHOGONAL TYPE
Cardiovascular
170d
Cleared
May 09, 1984
SWITCHING UNIT ELECTRODE CATHETER
Cardiovascular
131d
Cleared
Jan 14, 1983
SWITCHING UNIT ELECTRODE CATHETERS
Cardiovascular
66d
Cleared
Dec 29, 1981
TEMPERATURE PROBES
Cardiovascular
39d