D. E. Hokanson, Inc. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
D. E. Hokanson, Inc. has 19 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 19 cleared submissions from 1979 to 2004.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
19 devices
Cleared
Aug 06, 2004
POLYURETHANE BLOOD PRESSURE CUFFS
Cardiovascular
45d
Cleared
Dec 09, 2003
OB1 OBSTETRICAL DOPPLER
Radiology
70d
Cleared
Feb 12, 2003
A16 BLOOD FLOW MEASUREMENT SYSTEM
Cardiovascular
100d
Cleared
Aug 26, 1998
EC6 PLETHYSMOGRAPH
Cardiovascular
23d
Cleared
Aug 12, 1998
ANS 2000 ECG MONITOR AND RESPIRATION PACER
Cardiovascular
336d
Cleared
Oct 03, 1997
NIVP3 (WINDOWS VERSION OF NIVP
Cardiovascular
231d
Cleared
Feb 04, 1994
NON INVASIVE VASCULAR PROGRAM
General Hospital
239d
Cleared
Jan 13, 1994
EC 5R PLETHYSMOGRAPH
Anesthesiology
218d
Cleared
Nov 15, 1993
DISPOSABLE PENILE BLOOD PRESSURE CUFFS
Gastroenterology & Urology
158d
Cleared
Mar 06, 1991
E-20 RAPID CUFF INFLATOR
Cardiovascular
99d
Cleared
Oct 22, 1990
MODEL MD-5 DOPPLER
Cardiovascular
200d
Cleared
Jan 18, 1990
PROCORD MD3500 VASCULAR DIAGNOSTIC SYSTEM
Cardiovascular
94d
Cleared
Oct 28, 1988
3D VASCULAR RECORDER
Cardiovascular
43d
Cleared
Aug 19, 1988
ECG MONITOR AND RESPIRATION PACER
Cardiovascular
164d
Cleared
Oct 01, 1987
TL 400 TOTALAB VASCULAR DIAGNOSTIC SYSTEM
Cardiovascular
99d
Cleared
Mar 01, 1985
CALCULATING CUFF INFLATOR TD312
Cardiovascular
282d
Cleared
May 09, 1984
AUDIO BANDWIDTH ANALYZER
Radiology
99d
Cleared
Jul 08, 1980
EC-4 PLETHYSMOGRAPH
Cardiovascular
36d
Cleared
Dec 04, 1979
P-2 ULTRASONIC ARTERIOGRAPH
Cardiovascular
60d