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
1242226736
Device Listing 1242226736
Listing Summary
#
Listing key
1242226736
Premarket submission
K032087
Device
KEELER WIDE ANGLE OPHTHALMOSCOPE MODEL 1130-P-5004
Applicant
Keeler Instruments, Inc.
Product code
HLJ
Decision date
2003-11-26
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
15229
1000391004
1000391004
KEELER LTD.
1
N
2026-01-01
CLEWER HILL RD. WINDSOR, BERKSHIRE Windsor and Maidenhead GB SL4 4AA