GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC
GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC holds FDA 510(k) medical device clearances, first cleared 2016, most recent 2026.
Top product codes for GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC
Recent clearances by GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC
- K252718 — Lunar Astra
- K254161 — Automated Aortic Stenosis Software (AutoAS)
- K221148 — Vivid iq
- K203677 — ViewPoint 6
- K200158 — LOGIQ E10
- K191112 — GEHC DXA Bone Densitometers with enCORE version 18
- K181934 — Vivid T8, Vivid T9
- K180782 — Aria
- K170714 — Venue
- K170878 — Vivid S60N, Vivid S70N
- K161682 — GE Lunar DXA Bone Densitometers with enCORE version 17
- K161588 — Vscan Extend
- K161224 — LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3
- K153037 — LOGIQ V1/ LOGIQ V2
Data sourced from openFDA. This site is unofficial and independent of the FDA.