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
1557494018
Device Listing 1557494018
Listing Summary
#
Listing key
1557494018
Premarket submission
K030929
Device
ANA DETECT
Applicant
Orgentec Diagnostika GmbH
Product code
LJM
Decision date
2003-05-02
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
16128
3003232042
3003232042
ORGENTEC DIAGNOSTIKA GMBH
1
N
2026-01-01
CARL-ZEISS-STRASSE 49-51 MAINZ Rhineland-Palatinate DE 55129