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
1897193930
Device Listing 1897193930
Listing Summary
#
Listing key
1897193930
Premarket submission
K141638
Device
PROPPER INSIGHT BINOCULAR INDIRECT OPHTHALMOSOPE
Applicant
Propper Manufacturing Co., Inc.
Product code
HLI
Decision date
2014-09-17
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
36862
2410251
2410251
PROPPER MFG. CO., INC.
1
Y
2026-01-01
36-04 SKILLMAN AVE. Long Island City NY US 11101