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
1679348621
Device Listing 1679348621
Listing Summary
#
Listing key
1679348621
Premarket submission
K960874
Device
COMPLEMENT CONTROL
Applicant
Wako Chemicals USA, Inc.
Product code
JJX
Decision date
1996-06-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
232819
3005625991
3005625991
FUJIFILM Healthcare Americas Corporation
1
N
2026-01-01
1100 King Georges Post Rd Edison NJ US 08837