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
1053292907
Device Listing 1053292907
Listing Summary
#
Listing key
1053292907
Premarket submission
P190001
Device
therascreen PIK3CA RGQ PCR Kit
Applicant
QIAGEN GMBH
Product code
OWD
Decision date
2019-05-24
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