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
1898687592
Device Listing 1898687592
Listing Summary
#
Listing key
1898687592
Premarket submission
K103471
Device
UBM PLUS
Applicant
Accutome, Inc.
Product code
IYN
Decision date
2011-03-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
38248
2519784
2519784
KEELER INSTRUMENTS, INC.
1
Y
2020-04-25
3222 Phoenixville Pike Building #50 Malvern PA US 19355