Drager Medizintechnik GmbH

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K023289OPTION NIV, MODEL 8414115, UPGRADE KIT NIV, MODEL 8414072January 15, 2003
K010793OXYLOG 1000, MODEL 2M86840December 20, 2001
K012177VENTVIEW, MODEL 8414095September 4, 2001
K003068SAVINAJune 25, 2001
K010093NON-INVASIVE VENTILATION NIV OPTION, MODEL 84 14 474June 14, 2001
K010724SOLA 700,SOLA 500, SOLA 300June 7, 2001
K003067CALEODecember 13, 2000
K984611DRAGER SOLA SERIES, MODELS 1000/700/500/300March 29, 1999