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
1676423067
Device Listing 1676423067
Listing Summary
#
Listing key
1676423067
Premarket submission
K161502
Device
MC1 Plus
Applicant
General Project S.R.L.
Product code
IMI
Decision date
2016-08-16
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
17791
9710111
3002952153
CORNELIA DAMSKY
1
N
2020-04-25
6552 Hermosa Beach Ln Delray Beach FL US 33446