Draeger Medical AG & Co. KG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Draeger Medical AG & Co. KG - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Draeger Medical AG & Co. KG has 10 FDA 510(k) cleared anesthesiology devices. Based in Telford, US.
Historical record: 10 cleared submissions from 2008 to 2010.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Draeger Medical AG & Co. KG
10 devices
Cleared
Dec 10, 2010
VENTSTAR HEATED, INFINITY ID BREATHING CIRCUIT HEATED
Anesthesiology
88d
Cleared
Aug 06, 2010
VENTSTAR RESUSCITAIRE, MODEL MP00311, VENTSTAR RESUSCITAIRE CEU, MODEL MP00310
Anesthesiology
396d
Cleared
Apr 23, 2010
INFINITY MCABLE - MAINSTREAM CO2
Anesthesiology
18d
Cleared
Nov 24, 2009
NBP CUFF
Cardiovascular
57d
Cleared
Dec 29, 2008
EVITE XL
Anesthesiology
76d
Cleared
Oct 08, 2008
FOURTH GAS MODULE WITH CO2 FOR PRIMUS US APOLLO
Anesthesiology
139d
Cleared
Sep 22, 2008
CLASSICSTAR NV SE AND NOVASTAR NV SE AND AAV FULL FACE MASKS
Anesthesiology
95d
Cleared
Jul 30, 2008
FABIUS MRI
Anesthesiology
295d
Cleared
Apr 07, 2008
CARINA SYSTEM, MODEL 8419350
Anesthesiology
181d
Cleared
Jan 31, 2008
FILTER CARESTAR 30
General Hospital
192d