D. E. Hokanson, Inc.

FDA Regulatory Profile

D. E. Hokanson, Inc. appears in FDA public data with 0 recalls, 19 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Aug 6, 2004.

Summary

Total Recalls
0
510(k) Clearances
19
Inspections
0
Compliance Actions
0

Known Names

D. E. Hokanson, D E Hokanson

Recent 510(k) Clearances

K-NumberDeviceDate
K041689POLYURETHANE BLOOD PRESSURE CUFFSAug 6, 2004
K033156OB1 OBSTETRICAL DOPPLERDec 9, 2003
K023707A16 BLOOD FLOW MEASUREMENT SYSTEMFeb 12, 2003
K982707EC6 PLETHYSMOGRAPHAug 26, 1998
K973426ANS 2000 ECG MONITOR AND RESPIRATION PACERAug 12, 1998
K970570NIVP3 (WINDOWS VERSION OF NIVPOct 3, 1997
K932852NON INVASIVE VASCULAR PROGRAMFeb 4, 1994
K932812EC 5R PLETHYSMOGRAPHJan 13, 1994
K932851DISPOSABLE PENILE BLOOD PRESSURE CUFFSNov 15, 1993
K905367E-20 RAPID CUFF INFLATORMar 6, 1991
K901592MODEL MD-5 DOPPLEROct 22, 1990
K896034PROCORD MD3500 VASCULAR DIAGNOSTIC SYSTEMJan 18, 1990
K8839083D VASCULAR RECORDEROct 28, 1988
K881055ECG MONITOR AND RESPIRATION PACERAug 19, 1988
K872517TL 400 TOTALAB VASCULAR DIAGNOSTIC SYSTEMOct 1, 1987
K842067CALCULATING CUFF INFLATOR TD312Mar 1, 1985
K840402AUDIO BANDWIDTH ANALYZERMay 9, 1984
K801291EC-4 PLETHYSMOGRAPHJul 8, 1980
K792015P-2 ULTRASONIC ARTERIOGRAPHDec 4, 1979