FDA.reportPublic FDA data

Product code LKA

Device name
Culture Media, Antimicrobial Susceptibility Test
Medical specialty
Microbiology
Device class
2
Regulation number
866.1700
Review panel
MI
Implant
N
Life sustaining/supporting
N
GMP exempt
N
Third party review
Y
Summary malfunction reporting
Eligible
Source
FDA openFDA device classification dataset