Viasys Healthcare GmbH - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Viasys Healthcare GmbH has 14 FDA 510(k) cleared anesthesiology devices. Based in Yorba Linda, US.
Historical record: 14 cleared submissions from 2003 to 2009.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Sep 03, 2009
SPIROPRO
Anesthesiology
30d
Cleared
Aug 21, 2009
CLEAN PEAK FLOW METER
Anesthesiology
100d
Cleared
Jun 10, 2009
COR12+
Cardiovascular
20d
Cleared
May 18, 2009
MASTERSCREEN PAED - BABY BODY
Anesthesiology
325d
Cleared
Aug 20, 2008
VIP PULMONARY FUNCTION SYSTEM
Anesthesiology
177d
Cleared
Jun 26, 2008
FLOWSCREEN, FLOWSCREEN/CORSCREEN, FLOWSCREEN CT
Anesthesiology
104d
Cleared
Apr 22, 2008
MASTERSCREEN PFT, MASTERSCREEN PFT CT, MASTERSCREEN PFT BODY
Anesthesiology
270d
Cleared
Oct 10, 2007
MASTERSCREEN & OXYCON CPX
Anesthesiology
51d
Cleared
Aug 14, 2007
MASTERSCREEN PNEUMO & MASTERSCOPE
Anesthesiology
47d
Cleared
May 11, 2007
MODIFICATION TO FLOWSCREEN
Anesthesiology
298d
Cleared
May 04, 2007
CORSCREEN
Cardiovascular
60d
Cleared
Apr 07, 2004
MASTERSCREEN CPX AND OXYCON CPX
Anesthesiology
21d
Cleared
Nov 14, 2003
SPIROPRO SPO2
Anesthesiology
184d
Cleared
Jul 30, 2003
SPIROSOFT
Anesthesiology
105d