Acuson Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Acuson Corp. - FDA 510(k) Cleared Devices
Recent clearances: KINETDX PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM, CSV12 SOFTWARE VIEWER, SEQUOIA SIGNATURE II DIAGNOSTIC ULTRASOUND SYSTEM
37
Total
37
Cleared
0
Denied
Acuson Corp. has 37 FDA 510(k) cleared radiology devices. Based in Mountain View, US.
Historical record: 37 cleared submissions from 1988 to 2002.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Acuson Corp.
37 devices
Cleared
Nov 22, 2002
KINETDX PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM
Radiology
10d
Cleared
Oct 03, 2002
CSV12 SOFTWARE VIEWER
Radiology
30d
Cleared
Aug 13, 2002
SEQUOIA SIGNATURE II DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
11d
Cleared
Jul 09, 2002
CYPRESS ULTRASOUND SYSTEM
Radiology
61d
Cleared
Jun 27, 2001
CYPRESS SYSTEM
Radiology
90d
Cleared
Dec 01, 2000
3D ORGAN ASSESSMENT W/ MAGNETIC POSITION SENSING
Radiology
84d
Cleared
Dec 15, 1999
ACUNAV DIAGNOSTIC ULTRASOUND CATHETER
Radiology
131d
Cleared
Oct 18, 1999
FETAL ASSESSMENT CAP
Radiology
77d
Cleared
Aug 02, 1999
ASPEN ULTRASOUND WITH FREESTYLE IMAGING OPTION
Radiology
68d
Cleared
Dec 23, 1997
HARMONIC IMAGING WITH CONTRAST
Radiology
82d
Cleared
Nov 05, 1997
L7 TRANSDUCER USED ON ASPEN MODEL ULTRASOUND SYSTEM
Radiology
79d
Cleared
Mar 02, 1995
ACUSON MODEL 3001
Radiology
468d
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