6 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MODIFICATION TO IMMULITE MYOGLOBIN, MODEL LKMY1, LKMY5
FDA 510(k)
FDA Class 2
·Immunology
PATIENT EXAMINATION GLOVES (LATEX)
FDA 510(k)
FDA Class 1
·General Hospital
MODEL 6500 EXTRACTION IRRIGATION SYS
FDA 510(k)
FDA Class 1
·Obstetrics/Gynecology
ACCU-CHEK ® AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·March 6, 2013
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011
VIVA XT
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code NIK·August 8, 2014