7 results
·
26ms
·
Sources: EU EUDAMED, US FDA
APPLIC SYSTEM ACTIVATOR, ESPE
FDA 510(k)
FDA Class 1
·Dental
RX NC Takeru PTCA Balloon Dilatation Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
CLEVER CHEK HEALTH CARE SYSTEM SOFTWARE, VERSION 1.0
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ACCU-CHEK ACTIVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·November 13, 2007
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·October 3, 2012
ALLEGRETTO WAVE EYE-Q
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·December 19, 2013
TASUKI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LOX·June 6, 2019