Medical Device Manufacturer · US , Mchenry , IL

D. E. Hokanson, Inc. - FDA 510(k) Cleared Devices

19 submissions · 19 cleared · Since 1979

19

Total

19

Cleared

0

Denied

FDA 510(k) Regulatory Record - D. E. Hokanson, Inc. Cardiovascular ✕

14 devices

1-14 of 14

Cleared Aug 06, 2004

POLYURETHANE BLOOD PRESSURE CUFFS

Cardiovascular · 45d

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 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 Jul 08, 1980

EC-4 PLETHYSMOGRAPH

Cardiovascular · 36d

Cleared Dec 04, 1979

P-2 ULTRASONIC ARTERIOGRAPH

Cardiovascular · 60d