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
1971496356
Device Listing 1971496356
Listing Summary
#
Listing key
1971496356
Premarket submission
K091657
Device
IMMUNOSCAN CCPLUS
Applicant
Euro-Diagnostica AB
Product code
NHX
Decision date
2009-11-19
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
30845
1315336
1315336
IMMCO DIAGNOSTICS, INC.
1
N
2020-04-25
60 PINEVIEW DR. Amherst NY US 14228