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
1154431461
Device Listing 1154431461
Listing Summary
#
Listing key
1154431461
Premarket submission
K953939
Device
QUINTEST
Applicant
Bayer Corp.
Product code
SCL
Decision date
1995-11-13
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
44296
8043734
3004203341
David Lennarz
1
N
2026-01-01
144 Research Drive Hampton VA US 23666