5 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Country: United States
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ORTHOSISES DEVICES
FDA 510(k)
FDA Class 1
·Physical Medicine
PUTTY, ACCOE
FDA 510(k)
FDA Class 2
·Dental
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·June 12, 2007
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·January 3, 2014
TELIGEN
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 10, 2012