FDA 510(k) Applications Submitted by GE Medical Systems Ultrasound and Primary Care Diagnostic,
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K231989 | 07/05/2023 | LOGIQ E10s, LOGIQ Fortis | GE Medical Systems Ultrasound and Primary Care Diagnostic, |
| K232186 | 07/24/2023 | LOGIQ e | GE Medical Systems Ultrasound and Primary Care Diagnostic, |
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