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
1608079134
Device Listing 1608079134
Listing Summary
#
Listing key
1608079134
Premarket submission
K173145
Device
CereMetrix Silver
Applicant
Ceremetrix Corp
Product code
LLZ
Decision date
2018-02-28
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
217288
3014377024
3014377024
CEREMETRIX, CORP.
1
N
2020-04-25
991 Southpark Drive, Ste. 200 Littleton CO US 80120