Data / Medical devices / United States / D. E. Hokanson, Inc.

D. E. Hokanson, Inc.: FDA-registered device maker in Bellevue, WA, United States, 8 510(k) clearances

Name: D. E. Hokanson, Inc. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

D. E. Hokanson, Inc. is registered with the FDA (registration 3019130) in Bellevue, WA, United States. It lists 5 device types. The FDA files 8 510(k) clearances under its listings, the newest dated August 6, 2004. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3019130
Address: 12840 Ne 21ST PL, Bellevue, WA, United States, 98005
Owner or operator: D. E. HOKANSON, INC. (3019130)
Roles: Contract manufacturer, Manufacturer
First device listed: June 30, 1992
Registered through: 2026
Brand names listed: AG101 AIR SOURCE FOR E20, AI6 Arterial Inflow System, CC17(TM) Contoured Thigh Cuff, CC22(TM) Contoured Thigh Cuff, DP2 Disposable Digit or Penile Cuff, DP2.5 Disposable Digit or Penile Cuff, E-20 RAPID CUFF INFLATOR, EC-6 PLETHYSMOGRAPH and more

Devices it lists

Device	Product code	Class	Role	Source
Blood Pressure Cuff	DXQ	2	Contract manufacturer, Manufacturer	accessdata.fda.gov
Echocardiograph	DXK	2	Manufacturer	accessdata.fda.gov
Plethysmograph, Impedance	DSB	2	Manufacturer	accessdata.fda.gov
Plethysmograph, Photoelectric, Pneumatic Or Hydraulic	JOM	2	Manufacturer	accessdata.fda.gov
System, Measurement, Blood-Pressure, Non-Invasive	DXN	2	Contract manufacturer, Manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
August 6, 2004	K041689	POLYURETHANE BLOOD PRESSURE CUFFS	DXQ	Substantially Equivalent	D. E. Hokanson, Inc.	accessdata.fda.gov
February 12, 2003	K023707	A16 BLOOD FLOW MEASUREMENT SYSTEM	JOM	Substantially Equivalent	D. E. Hokanson, Inc.	accessdata.fda.gov
August 26, 1998	K982707	EC6 PLETHYSMOGRAPH	JOM	Substantially Equivalent	D. E. Hokanson, Inc.	accessdata.fda.gov
November 15, 1993	K932851	DISPOSABLE PENILE BLOOD PRESSURE CUFFS	DXQ	Substantially Equivalent	D. E. Hokanson, Inc.	accessdata.fda.gov
March 6, 1991	K905367	E-20 RAPID CUFF INFLATOR	DXN	Substantially Equivalent	D. E. Hokanson, Inc.	accessdata.fda.gov
October 22, 1990	K901592	MODEL MD-5 DOPPLER	DXK	Substantially Equivalent	D. E. Hokanson, Inc.	accessdata.fda.gov
January 18, 1990	K896034	PROCORD MD3500 VASCULAR DIAGNOSTIC SYSTEM	DSB	Substantially Equivalent	D. E. Hokanson, Inc.	accessdata.fda.gov
March 1, 1985	K842067	CALCULATING CUFF INFLATOR TD312	DXN	Substantially Equivalent	D. E. Hokanson, Inc.	accessdata.fda.gov

Compare with other makers

Updated August 6, 2004. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.