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
1390430216
Device Listing 1390430216
Listing Summary
#
Listing key
1390430216
Premarket submission
K172356
Device
BladderScan Prime PLUS System
Applicant
Verathon Incorporated
Product code
IYO
Decision date
2017-09-15
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
8696
3022472
3022472
Verathon Inc.
1
Y
2026-01-01
20001 North Creek Pkwy BOTHELL WA US 98011