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
1188673809
Device Listing 1188673809
Listing Summary
#
Listing key
1188673809
Premarket submission
K102400
Device
SYPHILIS HEALTH CHECK
Applicant
Diagnostics Direct, LLC
Product code
LIP
Decision date
2011-08-01
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
132433
3009178048
3009178048
DIAGNOSTICS DIRECT LLC
1
N
2026-01-01
373 96th St Unit C Stone Harbor NJ US 08247