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
1500907833
Device Listing 1500907833
Listing Summary
#
Listing key
1500907833
Premarket submission
K113319
Device
ROTOR-GENE Q MDX
Applicant
QIAGEN GmbH
Product code
OOI
Decision date
2012-02-06
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
71776
3005118020
3009391812
QIAGEN Manchester Ltd
1
N
2026-01-01
CityLabs 2.0 200 Hathersage Road Manchester Lancashire GB M13 0BH