Drager Medizintechnik GmbH
Drager Medizintechnik GmbH appears in FDA public data with 0 recalls, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 15, 2003.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K023289 | OPTION NIV, MODEL 8414115, UPGRADE KIT NIV, MODEL 8414072 | January 15, 2003 |
| K010793 | OXYLOG 1000, MODEL 2M86840 | December 20, 2001 |
| K012177 | VENTVIEW, MODEL 8414095 | September 4, 2001 |
| K003068 | SAVINA | June 25, 2001 |
| K010093 | NON-INVASIVE VENTILATION NIV OPTION, MODEL 84 14 474 | June 14, 2001 |
| K010724 | SOLA 700,SOLA 500, SOLA 300 | June 7, 2001 |
| K003067 | CALEO | December 13, 2000 |
| K984611 | DRAGER SOLA SERIES, MODELS 1000/700/500/300 | March 29, 1999 |