7 results
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27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
FIRST BEAT/CARDIO BEAT/CALC
FDA 510(k)
FDA Class 2
·Radiology
BREATH CONTROL GAME
FDA 510(k)
FDA Class 1
·Physical Medicine
MOBILLIFE - MODEL (MOBIL RAIZER 22) - POWER WHEELCHAIR
FDA 510(k)
FDA Class 2
·Physical Medicine
DENALI FEMORAL SYSTEM
FDA Adverse Event
Injury
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·May 27, 2014
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·January 30, 2013
RESTORE RECHARGEABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·January 12, 2011
WHITESTAR PHACO HANDPIECE
FDA Adverse Event
Malfunction
·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HQC·July 31, 2024