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
1297561240
Device Listing 1297561240
Listing Summary
#
Listing key
1297561240
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
47282
2247992
1000208827
Qfix
1
Y
2020-04-25
440 CHURCH ROAD Avondale PA US 19311