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
1599675673
Device Listing 1599675673
Listing Summary
#
Listing key
1599675673
Premarket submission
K935067
Device
AQUAPLAST
Applicant
Wfr/Aquaplast Corp.
Product code
IYE
Decision date
1994-05-26
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
310405
2247992
1000208827
Anholt Technologies Inc.
1
Y
2026-01-01
440 CHURCH ROAD Avondale PA US 19311