FDA 510(k) Applications Submitted by Martha Kamrow
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K210982 | 04/01/2021 | AMX Navigate | GE Medical Systems, LLC |
| K191112 | 04/26/2019 | GEHC DXA Bone Densitometers with enCORE version 18 | GE Medical Systems Ultrasound & Primary Care Diagnostics LLC |
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