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
1611883798
Device Listing 1611883798
Listing Summary
#
Listing key
1611883798
Premarket submission
K905069
Device
IODOSORB GEL
Applicant
Perstorp AB C/O Robert Joel Slomoff
Product code
KOZ
Decision date
1991-01-31
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
200900
8043792
3002808269
Becky Aldhizer
1
N
2026-01-01
5960 Heisley Road Mentor OH US 44060