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
1255704737
Device Listing 1255704737
Listing Summary
#
Listing key
1255704737
Premarket submission
K090668
Device
VISION TOOLS
Applicant
Millensys
Product code
LLZ
Decision date
2009-06-23
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
111078
3008177920
3008177920
Christine Nichols
1
N
2026-01-01
33 Lees Hill Road, Box 221 New Vernon NJ US 07976