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
1471045609
Device Listing 1471045609
Listing Summary
#
Listing key
1471045609
Premarket submission
K092538
Device
REFINE SUPPORT SYSTEM, MODEL 100.0100
Applicant
Alure Medical, Inc.
Product code
FTL
Decision date
2010-03-05
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
118881
9681572
3003263857
Bryan Blessing
1
N
2026-01-01
1207 Bangor St. San Diego CA US 92106