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
1702070305
Device Listing 1702070305
Listing Summary
#
Listing key
1702070305
Premarket submission
K143325
Device
OC-Light S FIT
Applicant
Eiken Chemical Co., Ltd.
Product code
KHE
Decision date
2015-08-20
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
43010
2435505
1000119795
POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC.
1
Y
2026-01-01
510 FURNACE DOCK RD. CORTLANDT MANOR NY US 10567