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
2068907025
Device Listing 2068907025
Listing Summary
#
Listing key
2068907025
Premarket submission
K182431
Device
Konicaminolta DI-X1
Applicant
Konica Minolta, Inc.
Product code
LLZ
Decision date
2018-11-26
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
14773
3003769120
3003769120
Jan Maniscalco
1
N
2026-01-01
411 Newark Pompton Turnpike Wayne NJ US 07470
14775
3004485675
3004485675
KONICA MINOLTA, INC.
1
N
2026-01-01
1 SAKURA-MACHI HINO-SHI Tokyo JP 191-8511
14774
3005406110
3005406110
KONICA MINOLTA TECHNOPRODUCTS CO., LTD.
1
N
2026-01-01
2-2-1 HIROSEDAI SAYAMA-SHI Saitama JP 350-1328