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
1360710294
Device Listing 1360710294
Listing Summary
#
Listing key
1360710294
Premarket submission
K133959
Device
PODIATRY X-RAY SYSTEM
Applicant
Source-Ray, Inc.
Product code
KPR
Decision date
2015-01-22
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
69434
3004606964
3004606964
Source-Ray, Inc.
1
N
2026-01-01
50 Fleetwood Ct Ronkonkoma NY US 11779