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
1903235850
Device Listing 1903235850
Listing Summary
#
Listing key
1903235850
Premarket submission
K960515
Device
PARAPAC
Applicant
Pneupac , Ltd.
Product code
BTL
Decision date
1996-10-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
219318
3013253796
3013253796
Paul Deku
1
N
2020-04-25
467 Erlanger Road Erlanger KY US 41018