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
1901376735
Device Listing 1901376735
Listing Summary
#
Listing key
1901376735
Premarket submission
K160846
Device
AmplifEYE
Applicant
Medivators, Inc.
Product code
FED
Decision date
2016-07-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
134207
1651395
3003012447
Medivators Inc
1
Y
2026-01-01
3150 Pollok Drive Conroe TX US 77303