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
1801680079
Device Listing 1801680079
Listing Summary
#
Listing key
1801680079
Premarket submission
K191194
Device
CLARUS
Applicant
Carl Zeiss Meditec, Inc.
Product code
QER
Decision date
2019-06-25
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
21273
2918630
2918630
CARL ZEISS MEDITEC INC
1
Y
2026-01-01
5300 Central Parkway DUBLIN CA US 94568