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Viasys Healthcare GmbH

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
17
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K092324SPIROPROSeptember 3, 2009
K091412CLEAN PEAK FLOW METERAugust 21, 2009
K091505COR12+June 10, 2009
K081823MASTERSCREEN PAED - BABY BODYMay 18, 2009
K080510VIP PULMONARY FUNCTION SYSTEMAugust 20, 2008
K080734FLOWSCREEN, FLOWSCREEN/CORSCREEN, FLOWSCREEN CTJune 26, 2008
K072061MASTERSCREEN PFT, MASTERSCREEN PFT CT, MASTERSCREEN PFT BODYApril 22, 2008
K072323MASTERSCREEN & OXYCON CPXOctober 10, 2007
K071753MASTERSCREEN PNEUMO & MASTERSCOPEAugust 14, 2007
K062011MODIFICATION TO FLOWSCREENMay 11, 2007
K070614CORSCREENMay 4, 2007
K060421SONARA; SONARA/TEKNovember 3, 2006
K040698MASTERSCREEN CPX AND OXYCON CPXApril 7, 2004
K031515SPIROPRO SPO2November 14, 2003
K031713AUDIOMETER, OTOACOUSTIC EMISSION, AUDITORY BRANSTEM RESPONSE ACCESSAugust 12, 2003
K030517BALL RECORDING ELECTRODE/STIMULATION PROBEAugust 1, 2003
K031194SPIROSOFTJuly 30, 2003