7 results
·
25ms
·
Sources: EU EUDAMED, US FDA
A&D AUTOMATIC DIGITAL BLOOD PRESSURE METER 2510/20
FDA 510(k)
FDA Class 2
·Cardiovascular
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690128014·AK3 PS-R Insert Trial Size 4, 28mm
PATIENT EXAMINATION GLOVES (LATEX) (POWDERED)
FDA 510(k)
FDA Class 1
·General Hospital
DELFIA PROGESTERONE KIT
FDA 510(k)
FDA Class 1
·Clinical Chemistry
PRECISION XTRA
FDA Adverse Event
Injury
·Product code NBW·June 25, 2014
COULTER AC*T DIFF 2 ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code GKZ·January 3, 2013
OCTRODE PERCUTANEOUS LEAD
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·November 4, 2010