7 results
·
26ms
·
Sources: EU EUDAMED, US FDA
PHARMASEED, MODEL BT-125-2
FDA 510(k)
FDA Class 2
·Radiology
GYNECARE X-TRACT MORCELLATOR
FDA Adverse Event
Injury
·ETHICON, INC.·Product code HET·June 8, 2006
SLT CONTACT LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
XPRESS
FDA 510(k)
FDA Class 2
·Radiology
FLOGARD
FDA Adverse Event
Malfunction
·SHARP CORPORATION OSAKA JAPAN·Product code FRN·March 7, 2013
UNKNOWN -- IOL
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·February 11, 2011
SPRINT
FDA Adverse Event
Malfunction
·MPRI·Product code LWS·August 8, 2014