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
1224742971
Device Listing 1224742971
Listing Summary
#
Listing key
1224742971
Premarket submission
K143257
Device
KrystalRad 11000 and KrystalRad 3000 Digital Stationary Radiographic System
Applicant
Medicatech USA
Product code
KPR
Decision date
2015-02-06
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
65156
3004989804
3004989804
MEDICATECH USA
1
N
2026-01-01
1245 N Patt St Anaheim CA US 92801