Burdick Corp. - FDA 510(k) Cleared Devices
38
Total
38
Cleared
0
Denied
Burdick Corp. has 38 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 38 cleared submissions from 1976 to 1994.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
38 devices
Cleared
Dec 05, 1994
ALTAIR-DISC RECORDER
Cardiovascular
188d
Cleared
Oct 13, 1994
BURDICK PRO2 OXIMETER
Anesthesiology
205d
Cleared
Jul 24, 1991
E560 ELECTROCARDIOGRAPH
Cardiovascular
351d
Cleared
Jul 24, 1991
ELITE II ELECTROCARDIOGRAPH
Cardiovascular
327d
Cleared
Jun 08, 1990
NEOSERV 824
Orthopedic
113d
Cleared
Oct 03, 1989
ERGOMED 840/ERGOMED 840L
Cardiovascular
298d
Cleared
Jun 01, 1989
E350 ELECTROCARDIOGRAPH
Cardiovascular
44d
Cleared
Jan 17, 1989
E550 ELECTROCARDIOGRAPH
Cardiovascular
155d
Cleared
Nov 06, 1987
M300 MONITOR/CONTROLLER T500 TREADMILL
Cardiovascular
51d
Cleared
Apr 13, 1987
ELITE ELECTROCARDIOGRAPH
Cardiovascular
38d
Cleared
Apr 09, 1987
EK10 ELECTROCARDIOGRAPH
Cardiovascular
36d
Cleared
May 02, 1986
595 ARRHYTHMIA MONITORING SYSTEM
Cardiovascular
344d
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