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
1969702614
Device Listing 1969702614
Listing Summary
#
Listing key
1969702614
Premarket submission
K090422
Device
LUCAS 2
Applicant
Jolife AB
Product code
DRM
Decision date
2009-06-17
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
220976
3010030355
3010030355
PHYSIO-CONTROL MAASTRICHT, INC.
1
N
2026-01-01
Gaetano Martinolaan 50 Maastricht Limburg NL 6229 GS