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
1896064395
Device Listing 1896064395
Listing Summary
#
Listing key
1896064395
Premarket submission
K092329
Device
SOPIX 2
Applicant
Sopro
Product code
MUH
Decision date
2010-07-20
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
13320
9615782
3004084693
Noelle Zuccarello
1
N
2026-01-01
1001 Briggs Rd Mount Laurel NJ US 08054