Medical Device Manufacturer · US , Wheeling , IL

Viasys Medsystems - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2004

7

Total

7

Cleared

0

Denied

Viasys Medsystems has 7 FDA 510(k) cleared medical devices. Based in Wheeling, US.

Historical record: 7 cleared submissions from 2004 to 2008. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Viasys Medsystems Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Viasys Medsystems

7 devices

1-7 of 7

Cleared Nov 07, 2008

ENTERAL PUMP SET, MODEL 20-1010

Gastroenterology & Urology · 142d

Cleared Jun 27, 2008

MODIFICATION TO CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900

Gastroenterology & Urology · 109d

Cleared Apr 02, 2007

CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900

Gastroenterology & Urology · 179d

Cleared May 06, 2005

ANTI-I.V. ENTERAL FEEDING SYSTEM

Gastroenterology & Urology · 183d

Cleared Mar 25, 2005

PULMANEX DISPOSABLE PRESSURE MANOMETER, MODEL 50-5000

Anesthesiology · 45d

Cleared Mar 16, 2005

STACKHOUSE FREEDOMAIRE II SURGICAL HELMET SYSTEM, MODELS 12000, 12010, 12011,...

General Hospital · 135d

Cleared Dec 17, 2004

Gastroenterology & Urology · 147d