D. E. Hokanson, Inc.
FDA 510(k) medical device clearances.
Top product codes for D. E. Hokanson, Inc.
Recent clearances by D. E. Hokanson, Inc.
- K041689 — POLYURETHANE BLOOD PRESSURE CUFFS
- K033156 — OB1 OBSTETRICAL DOPPLER
- K023707 — A16 BLOOD FLOW MEASUREMENT SYSTEM
- K982707 — EC6 PLETHYSMOGRAPH
- K973426 — ANS 2000 ECG MONITOR AND RESPIRATION PACER
- K970570 — NIVP3 (WINDOWS VERSION OF NIVP
- K932852 — NON INVASIVE VASCULAR PROGRAM
- K932812 — EC 5R PLETHYSMOGRAPH
- K932851 — DISPOSABLE PENILE BLOOD PRESSURE CUFFS
- K905367 — E-20 RAPID CUFF INFLATOR
- K901592 — MODEL MD-5 DOPPLER
- K896034 — PROCORD MD3500 VASCULAR DIAGNOSTIC SYSTEM
- K883908 — 3D VASCULAR RECORDER
- K881055 — ECG MONITOR AND RESPIRATION PACER
- K872517 — TL 400 TOTALAB VASCULAR DIAGNOSTIC SYSTEM
- K842067 — CALCULATING CUFF INFLATOR TD312
- K840402 — AUDIO BANDWIDTH ANALYZER
- K801291 — EC-4 PLETHYSMOGRAPH
- K792015 — P-2 ULTRASONIC ARTERIOGRAPH
Data sourced from openFDA. This site is unofficial and independent of the FDA.