Medical Device Manufacturer · US , Kirkland , WA

Diagnostic Ultrasound Corp. - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1985

Recent clearances: DIAGNOSTIC ULTRASOUND BLADDERMASS BVM 6500 ULTRASOUND SYSTEM, BLADDERSCAN BVI 6100, BLADDERMANAGER PCI 5000 MODEL 1002

Total

Cleared

Denied

Diagnostic Ultrasound Corp. has 16 FDA 510(k) cleared medical devices. Based in Kirkland, US.

Historical record: 16 cleared submissions from 1985 to 2003. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Diagnostic Ultrasound Corp. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Tuv America, Inc. and Tuv Rheinland of North America, Inc..

Diagnostic Ultrasound Corp. is one of 15128 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Diagnostic Ultrasound Corp.

16 devices

1-12 of 16

Cleared Mar 26, 2003

DIAGNOSTIC ULTRASOUND BLADDERMASS BVM 6500 ULTRASOUND SYSTEM

BLADDERMANAGER PCI 5000 MODEL 1002

K982568 · ITX

Radiology · 186d

Cleared Oct 01, 1996

BLADDER MANAGER PCI 5000, BLADDERSCAN BVI 5000

K963585 · IYO

Radiology · 22d

Cleared May 24, 1996

BLADDERMANAGER PCI 5000 / BLADDERSCAN BVI 5000

DIAGNOSTIC ULTRASOUND/URO-GYN UPS 2020, GI VERSION

K920664 · FFX

Gastroenterology & Urology · 679d

DIAGNOSTIC ULTRASOUND/URO-GYN UPS 2020

K911125 · FAP

Gastroenterology & Urology · 155d

Cleared Aug 15, 1991

DIAGNOSTIC ULTRASOUND/URO-GYN UD 511

K911166 · DXT

Gastroenterology & Urology · 153d

Cleared Jun 10, 1991

DIAGNOSTIC ULTRASOUND/URO-GYN UDS 2000 SERIES

K911091 · FAP

Gastroenterology & Urology · 90d

Diagnostic Ultrasound Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Diagnostic Ultrasound Corp.

Filters