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
1078236401
Device Listing 1078236401
Listing Summary
#
Listing key
1078236401
Premarket submission
K091343
Device
MRI NEURO DRAPE
Applicant
Surgivision, Inc.
Product code
KKX
Decision date
2009-09-22
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
14811
8043817
3003094575
MICROTEK DOMINICANA, S.A.
1
N
2020-04-25
ZONA FRANCA No. 2 LA ROMANA La Romana DO --