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
1941217386
Device Listing 1941217386
Listing Summary
#
Listing key
1941217386
Premarket submission
K971103
Device
AIA NEXIA-AUTOMATED ENZYME IMMUNOASSAY SYSTEM
Applicant
Tosoh Medics, Inc.
Product code
KHO
Decision date
1997-06-27
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
134960
3006198300
3006198300
Kathy Fisher
1
N
2026-01-01
333 Fiske St Holliston MA US 01746