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
1725203696
Device Listing 1725203696
Listing Summary
#
Listing key
1725203696
Premarket submission
K243331
Device
LVivo Seamless
Applicant
Dia Imaging Analysis, Ltd.
Product code
QIH
Decision date
2025-03-06
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
1227
3019216
3019216
Philips Ultrasound LLC
1
Y
2026-01-01
22100 Bothell Everett Hwy BOTHELL WA US 98021
343942
3010656400
3010656400
Ondrea Bermudez
1
N
2026-01-01
3721 VALLEY CENTRE DR San Diego CA US 92130