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
1111013452
Device Listing 1111013452
Listing Summary
#
Listing key
1111013452
Premarket submission
K002476
Device
LUMBOPERITONEAL SHUNT SYSTEM
Applicant
Phoenix Biomedical Corp.
Product code
JXG
Decision date
2000-11-09
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
79600
3001587388
3001587388
SOPHYSA
1
N
2026-01-01
05 RUE GUY MOQUET ORSAY, CEDEX Essonne FR 91400