FDA.reportPublic FDA data

Device Listing 2054568989

Listing Summary#

Listing key
2054568989
Premarket submission
K060788
Device
TRIAGE TOX DRUG SCREEN CONTROL LEVEL 1 MODEL 94413 AND LEVEL 2 MODEL 94414
Applicant
Biosite Incorporated
Product code
DIF
Decision date
2006-07-10