FDA 510(k) Applications Submitted by Shlomit Segman
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K140381 |
02/14/2014 |
SENSILIGHT/ SENSILIGHT PLUS |
EL GLOBAL TRADE LTD. |
K220467 |
02/17/2022 |
The Family of UltraPulse CO2 Surgical and Aesthetic Lasers, Delivery Devices and Accessories |
Lumenis Be, Ltd. |
K140527 |
03/04/2014 |
SENSILIGHT MINI |
EL GLOBAL TRADE LTD. |
K220877 |
03/25/2022 |
Selecta Duet LED, Digital Duet, Selecta LED Trio, Digital Trio Laser Systems |
Lumenis Be, Inc. |
DEN200028 |
04/20/2020 |
Lumenis Stellar M22 |
Lumenis Ltd. |
K201663 |
06/19/2020 |
AcuPulse W CO2 Laser Systems, Delivery Devices and Accessories |
Lumenis Ltd. |
K202428 |
08/25/2020 |
AcuPulse W CO2 Laser Systems, Delivery Devices and Accessories |
Lumenis Ltd. |
K212703 |
08/26/2021 |
AcuPulse CO2 Laser System, Delivery Devices and Accessories |
Lumenis, Ltd. |
K222790 |
09/15/2022 |
F65 Laser System |
Lumenis Be, Ltd. |
K203544 |
12/04/2020 |
UltraPulse Surgical and Aesthetic CO2 Laser System, Delivery Devices and Accessories |
Lumenis Ltd. |
K193500 |
12/17/2019 |
Stellar M22 for Intense Pulsed Light (IPL) and Laser System |
Lumenis Ltd. |
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