FDA.reportPublic FDA data

Device Listing 1228006311

Listing Summary#

Listing key
1228006311
Premarket submission
K260673
Device
LOGIQ Vita; LOGIQ Vita Pro; LOGIQ Vita Express; LOGIQ Vita Plus; LOGIQ Vita Power; LOGIQ S20; LOGIQ S20 Pro; LOGIQ S20 Express; LOGIQ S20 Plus; LOGIQ S20 Power
Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostics
Product code
IYN
Decision date
2026-03-24