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
1984811986
Device Listing 1984811986
Listing Summary
#
Listing key
1984811986
Premarket submission
K940952
Device
UMBILI-CATH-S-DL
Applicant
Gesco Intl., Inc.
Product code
FOS
Decision date
1994-07-29
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
32841
1718873
1718873
UTAH MEDICAL PRODUCTS, INC.
1
Y
2026-01-01
7043 South 300 West Midvale UT US 84047