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
1456837010
Device Listing 1456837010
Listing Summary
#
Listing key
1456837010
Premarket submission
K143721
Device
PRCT2
Applicant
Fx Solutions
Product code
HRS
Decision date
2015-08-27
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
194656
3013096318
3013096318
Kathy Trier
1
N
2020-04-25
13465 Midway road Dallas TX US 75244