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
1952420886
Device Listing 1952420886
Listing Summary
#
Listing key
1952420886
Premarket submission
K963609
Device
PHASE PLUS
Applicant
Zhermack S.P.A.
Product code
ELW
Decision date
1996-11-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
212059
9614794
3003762341
ZHERMACK S.P.A.
1
N
2026-01-01
VIA BOVAZECCHINO, 100 BADIA POLESINE (RO) Rovigo IT 45021