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
1706262343
Device Listing 1706262343
Listing Summary
#
Listing key
1706262343
Premarket submission
K950461
Device
WELCH ALLYN OPHTHALMOSCOPE
Applicant
Welch Allyn, Inc.
Product code
HLI
Decision date
1995-04-04
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
188431
1316463
1316463
WELCH ALLYN, INC.
1
Y
2020-04-25
4341 STATE STREET RD. Skaneateles Falls NY US 13153