Drager Medizintechnik GmbH
Telford, PA, US
Drager Medizintechnik GmbH appears in FDA device records in Telford, PA. FDA records list 8 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 8
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 8 510(k) clearances for Drager Medizintechnik GmbH between 1999 and 2003. The busiest year on record is 2001, with 5. The most recent is 2003, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1999 | 1 |
| 2000 | 1 |
| 2001 | 5 |
| 2003 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K023289 | OPTION NIV, MODEL 8414115, UPGRADE KIT NIV, MODEL 8414072 | CBK | Substantially Equivalent | |
| K010793 | OXYLOG 1000, MODEL 2M86840 | CBK | Substantially Equivalent | |
| K012177 | VENTVIEW, MODEL 8414095 | CBK | Substantially Equivalent | |
| K003068 | SAVINA | CBK | Substantially Equivalent | |
| K010093 | NON-INVASIVE VENTILATION NIV OPTION, MODEL 84 14 474 | CBK | Substantially Equivalent | |
| K010724 | SOLA 700,SOLA 500, SOLA 300 | FTD | Substantially Equivalent | |
| K003067 | CALEO | FMZ | Substantially Equivalent | |
| K984611 | DRAGER SOLA SERIES, MODELS 1000/700/500/300 | FSY | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain