Medical Device Manufacturer · US , Mountain View , CA

Acuson Corp. - FDA 510(k) Cleared Devices

37 submissions · 37 cleared · Since 1988

Total

Cleared

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.

FDA 510(k) Regulatory Record - Acuson Corp.

37 devices

1-12 of 37

Cleared Nov 22, 2002

KINETDX PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM

K023772 · LLZ

Radiology · 10d

Cleared Oct 03, 2002

CSV12 SOFTWARE VIEWER

K022896 · LLZ

Radiology · 30d

Cleared Aug 13, 2002

SEQUOIA SIGNATURE II DIAGNOSTIC ULTRASOUND SYSTEM

K022567 · IYN

Radiology · 11d

Cleared Jul 09, 2002

CYPRESS ULTRASOUND SYSTEM

3D ORGAN ASSESSMENT W/ MAGNETIC POSITION SENSING

K002807 · IYO

Radiology · 84d

Cleared Dec 15, 1999

ACUNAV DIAGNOSTIC ULTRASOUND CATHETER

ASPEN ULTRASOUND WITH FREESTYLE IMAGING OPTION

K991805 · IYN

Radiology · 68d

Cleared Dec 23, 1997

HARMONIC IMAGING WITH CONTRAST

K973767 · IYO

Radiology · 82d

Cleared Nov 05, 1997

L7 TRANSDUCER USED ON ASPEN MODEL ULTRASOUND SYSTEM

Looking for a specific device from Acuson Corp.? Search by device name or K-number.

Search all Acuson Corp. devices

Acuson Corp. - FDA 510(k) Cleared Devices

Filters