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
1538434500
Device Listing 1538434500
Listing Summary
#
Listing key
1538434500
Premarket submission
K092837
Device
OTI-SCAN 3000
Applicant
Opko Instrumentation, Inc.
Product code
IYO
Decision date
2009-12-23
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
162648
3005744933
3005744933
Optos Inc.
1
N
2026-01-01
155 Northboro Rd Ste 12 Southborough MA US 01772