Medical Device Manufacturer · DE , Hoechberg

Carefusion Germany 234 GmbH - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 2010

Recent clearances: Sentry WEB SmartInterp, Vyntus / SentrySuite Product Line, Vyntus Walk

View 12 510(k) Devices ↓

12

Total

12

Cleared

0

Denied

FDA 510(k) Regulatory Record - Carefusion Germany 234 GmbH Anesthesiology ✕

10 devices

1-10 of 10

Cleared Aug 14, 2015

Vyntus / SentrySuite Product Line

Anesthesiology · 141d

Cleared Mar 20, 2015

Anesthesiology · 157d

Cleared Dec 29, 2014

MICROBLAB, MICROLOOP

Anesthesiology · 165d

Cleared Aug 22, 2014

VYNTUS/ SENTRYSUITE PRODUCT LINE

Anesthesiology · 242d

Cleared Nov 19, 2012

SENTRYSUITE PRODUCT LINE

Anesthesiology · 76d

Cleared May 10, 2012

SENTRYSUITE PRODUCT LINE

Anesthesiology · 139d

Cleared Apr 13, 2012

Anesthesiology · 177d

Cleared Aug 12, 2011

SENTRYSUITE PRODUCT LINE

Anesthesiology · 119d

Cleared Feb 10, 2011

MASTERSCREEN IOS

Anesthesiology · 219d

Cleared Jan 13, 2010

ASTHMA MONITOR AM3

Anesthesiology · 114d