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
1351884109
Device Listing 1351884109
Listing Summary
#
Listing key
1351884109
Premarket submission
K883968
Device
TENDERFOOT
Applicant
International Technidyne Corp.
Product code
FMK
Decision date
1988-12-01
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
177278
3002721930
2250033
Accriva Diagnostics, Inc.
1
N
2026-01-01
6260 Sequence Drive San Diego CA US 92121