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
1541368191
Device Listing 1541368191
Listing Summary
#
Listing key
1541368191
Premarket submission
K032150
Device
SAFETY-MULTIFLY
Applicant
Sarstedt, Inc.
Product code
FPA
Decision date
2003-09-12
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
39876
9617475
3002808075
Susan Smith
1
N
2026-01-01
1025 Saint James Church Rd Newton NC US 28658