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Acuson Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
37
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K023772KINETDX PICTURE ARCHIVING AND COMMUNICATIONS SYSTEMNovember 22, 2002
K022896CSV12 SOFTWARE VIEWEROctober 3, 2002
K022567SEQUOIA SIGNATURE II DIAGNOSTIC ULTRASOUND SYSTEMAugust 13, 2002
K021497CYPRESS ULTRASOUND SYSTEMJuly 9, 2002
K010950CYPRESS SYSTEMJune 27, 2001
K0028073D ORGAN ASSESSMENT W/ MAGNETIC POSITION SENSINGDecember 1, 2000
K992631ACUNAV DIAGNOSTIC ULTRASOUND CATHETERDecember 15, 1999
K992580FETAL ASSESSMENT CAPOctober 18, 1999
K991805ASPEN ULTRASOUND WITH FREESTYLE IMAGING OPTIONAugust 2, 1999
K973767HARMONIC IMAGING WITH CONTRASTDecember 23, 1997
K973079L7 TRANSDUCER USED ON ASPEN MODEL ULTRASOUND SYSTEMNovember 5, 1997
K942296V5MMarch 2, 1995
K935595ACUSON MODEL 3001March 2, 1995
K930964ACUSON MODEL #29001 (DIAGNOSTIC ULTRASOUND DEVICE)October 26, 1994
K934915ACUSON MODEL 2001October 21, 1994
K940285ACUSON PICTURE ARCHIVING & COMMUNICATION SYSTEM MODIFICATIONApril 29, 1994
K933663MODIFICATION OF ACUSON V510B TRANSDUCERJanuary 21, 1994
K920882ACUSON V714 TRANSDUCERMarch 26, 1993
K921341ACUSON V714OR TRANSDUCERNovember 27, 1992
K902515ACUSON S228 TRANSDUCER FOR TRANSCRANIAL COLOR DOPPSeptember 4, 1992