6 results
·
26ms
·
Sources: EU EUDAMED, US FDA
NU-THOR THORACOSTOMY KIT
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Scrambler Therapy MC-5 A Device
FDA 510(k)
FDA Class 2
·Neurology
LUTH-ALL SUB-Q NEEDLE SET
FDA 510(k)
FDA Class 2
·General Hospital
HANA FEMORAL LIFT
FDA Adverse Event
Malfunction
·MIZUHO ORTHOPEDIC SYSTEMS, INC·Product code JEA·May 27, 2014
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·November 21, 2012
ITREL 3
FDA Adverse Event
Malfunction
·MED REL, HUMACAO·Product code LGW·September 1, 2010