Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1181731988
Device Listing 1181731988
Listing Summary
#
Listing key
1181731988
Premarket submission
P190026
Device
therascreen BRAF V600E RGQ PCR Kit
Applicant
QIAGEN GmbH
Product code
OWD
Decision date
2020-04-15
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
23249
3004013603
3004013603
QIAGEN, GMBH
1
N
2026-01-01
QIAGEN STRASSE 1 HILDEN North Rhine-Westphalia DE 40724