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
1979859714
Device Listing 1979859714
Listing Summary
#
Listing key
1979859714
Premarket submission
K160004
Device
Crosstella OTW
Applicant
KANEKA Corporation
Product code
LIT
Decision date
2016-04-29
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
45439
9614654
3002808904
Audra bogucki
1
N
2026-01-01
623 FIFTH AVE., NEW YORK NY US 10022