EchoPAC Software Only, EchoPAC Plug-in— 510(k) K220940

Substantially Equivalent

GE Medical Systems Ultrasound and Primary Care Diagnostics

FDA 510(k) clearance K220940 for EchoPAC Software Only, EchoPAC Plug-in, Substantially Equivalent on 2022-07-22. Applicant: GE Medical Systems Ultrasound and Primary Care Diagnostics.

Clearance details

Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostics
Product code
Code QIH
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Wauwatosa, WI, US
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