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
1716023495
Device Listing 1716023495
Listing Summary
#
Listing key
1716023495
Premarket submission
K061404
Device
MONO-CRAWFORD NASO-LACRIMAL INTUBATION DEVICE
Applicant
Fci Ophthalmics, Inc.
Product code
OKS
Decision date
2006-08-07
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
21279
9615745
3000314405
Paul Swift
1
N
2026-01-01
5300 Central Pkwy Dublin CA US 94568
21269
3002991496
3002991496
Paul Swift
1
N
2026-01-01
5300 Central Pkwy Dublin CA US 94568
21271
3004467263
3004467263
Paul Swift
1
N
2026-01-01
5300 Central Pkwy Dublin CA US 94568