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
1934277880
Device Listing 1934277880
Listing Summary
#
Listing key
1934277880
Premarket submission
K962015
Device
RHEUMATOID FACTOR (RF) REAGENTI A LATEX SLIDE TEST
Applicant
Teco Diagnostics
Product code
DHR
Decision date
1996-11-25
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
90323
3005146313
3005146313
SANZAY CORPORATION -
1
N
2026-01-01
1080 NW 163rd Drive Miami Gardens FL US 33169