Medical Device Manufacturer · US , Telford , PA

Drager Medizintechnik GmbH - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1999

Recent clearances: OPTION NIV, MODEL 8414115, UPGRADE KIT NIV, MODEL 8414072, OXYLOG 1000, MODEL 2M86840, VENTVIEW, MODEL 8414095

View 8 510(k) Devices ↓

8

Total

8

Cleared

0

Denied

FDA 510(k) Regulatory Record - Drager Medizintechnik GmbH General Hospital ✕

1 devices

1-1 of 1

Cleared Dec 13, 2000

General Hospital · 72d