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
1646118306
Device Listing 1646118306
Listing Summary
#
Listing key
1646118306
Premarket submission
K211301
Device
Pathfinder Endoscope Overtube
Applicant
Neptune Medical, Inc.
Product code
FED
Decision date
2021-05-28
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
233970
3015451828
3015451828
NEPTUNE MEDICAL, INC
1
N
2026-01-01
1828 El Camino Real 5th Floor Burlingame CA US 94010