6 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NuFACE Mini Device
FDA 510(k)
FDA Class 2
·Neurology
MAX ORIENT SUCTION DEVICE FOR ELECTROCAUTERIZER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DISPOSABLE GROUNDING PAD SERIES AND ELECTRODE SERIES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·October 22, 2014
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·August 4, 2011
MECHANICAL WALKER, ROLLATOR
FDA Adverse Event
KENSTONE METAL·Product code ITJ·June 26, 2013