6 results
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20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Turbo-Power Laser Atherectomy Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
MODIFICATION TO XIA SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
HYDROCOIL(R) EMBOLIC SYSTEM (HES)
FDA 510(k)
FDA Class 2
·Neurology
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE REHABILITATION EQUIP·Product code ITI·October 8, 2014
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·July 7, 2011
URETEX TO2 URETHRAL SUPPORT SYSTEM
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION·Product code OTN·May 16, 2013