6 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS
FDA 510(k)
FDA Class 2
·Orthopedic
STRATUS(R) IMMUNOASSAY CONTROLS LEVELS I, II, III
FDA 510(k)
FDA Class 1
·Clinical Toxicology
OXYGEN, AIR, VACUUM & NITROUS-OXIDE COUPLERS
FDA 510(k)
FDA Class 1
·Anesthesiology
POSEY KEEPSAFE DELUXE
FDA Adverse Event
Malfunction
·J. T. POSEY CO.·Product code KMI·January 18, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·August 4, 2014
PRECISION TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011