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
1127295548
Device Listing 1127295548
Listing Summary
#
Listing key
1127295548
Premarket submission
K972698
Device
TOF-WATCH
Applicant
Organon Teknika Corp.
Product code
KOI
Decision date
1997-12-16
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
215638
3014288445
3014288445
Foram S Devdhara
1
N
2020-04-25
1180 Church Road- Suite 1 Lansdale PA US 19446