FDA 510(k) Applications Submitted by Karin Shimoni

FDA 510(k) Number Submission Date Device Name Applicant
K240053 01/08/2024 Venue Go GE Medical Systems Ultrasound and Primary Care Diagnostics
K240111 01/16/2024 Venue GE Medical Systems Ultrasound and Primary Care Diagnostics
K240206 01/25/2024 Venue Sprint GE Medical Systems Ultrasound and Primary Care Diagnostics
K251322 04/29/2025 Venue; Venue Go; Venue Fit; Venue Sprint GE Medical Systems Ultrasound and Primary care Diagnostics,
K234106 12/26/2023 Venue Fit GE Medical Systems Ultrasound and Primary Care Diagnostics


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