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
1876304186
Device Listing 1876304186
Listing Summary
#
Listing key
1876304186
Premarket submission
K152317
Device
Stretta Catheter
Applicant
Mederi Therapeutics, Inc.
Product code
GEI
Decision date
2015-09-23
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
341190
3039167637
3039167637
THE REFLUX COMPANY
1
N
2026-01-01
7868 Silverton Ave Ste J San Diego CA US 92126