FDA.reportPublic FDA data

Device Listing 1624035742

Listing Summary#

Listing key
1624035742
Premarket submission
DEN200072
Device
Lumipulse G ß-Amyloid Ratio (1-42/1-40)
Applicant
Fujirebio Diagnostics,Inc.
Product code
QSE
Decision date
2022-05-04