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
1481017100
Device Listing 1481017100
Listing Summary
#
Listing key
1481017100
Premarket submission
K860285
Device
XRO GASTRO-DUODENAL, DUAL FLOW TUBE, SALEM TYPE
Applicant
Vygon Corp.
Product code
KNT
Decision date
1986-02-11
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
9748
8020785
3009291251
Chris Steinke
1
N
2026-01-01
87 Venture Dr Dover NH US 03820
220305
3002808467
3002808467
Dimequip
1
N
2026-01-01
Route de Bavay Frameries Hainaut BE 7080
220310
3011237770
3011237770
Vygon Verneuil
1
N
2026-01-01
Parc Alata 5 Avenue des Bouleaux Verneuil En Halatte Oise FR 60550