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
1658784561
Device Listing 1658784561
Listing Summary
#
Listing key
1658784561
Premarket submission
K111534
Device
ABACUS 3CP
Applicant
Diatron U.S., Inc.
Product code
GKZ
Decision date
2012-08-02
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