6 results
·
22ms
·
Sources: EU EUDAMED, US FDA
DIGMI-2000 (GSI INTERNAL REFERENCE)/LD2800 (MARKETING NAME)
FDA 510(k)
FDA Class 2
·Radiology
Comprehensive Segmental Revision System (SRS)
FDA 510(k)
FDA Class 2
·Orthopedic
LITEDUO
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
RIATA ACTIVE FIXATION
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·February 21, 2013
FREESTYLE FREEDOM LITE
FDA Adverse Event
Injury
·ABBOTT DIABETES CARE INC.·Product code NBW·January 30, 2011
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·August 1, 2014