FDA 510(k) Applications Submitted by Amaya De Levie
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K180597 | 03/06/2018 | AcuPulse (previously called AcuPulse 30/40 ST); AcuPulse 40W G; AcuPulse DUO | Lumenis Ltd. |
| K170179 | 01/19/2017 | LightSheer Desire; LightSheer Desire Light; LightSheer Duet; LightSheer Infinity | Lumenis Ltd. |
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