FDA 510(k) Applications Submitted by Livsmed Inc.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K220384	02/10/2022	ArtiSential Laparoscopic Instruments-Electrodes	LivsMed Inc.
K200875	04/01/2020	ArtiSential Laparoscopic Instruments - Electrodes	LivsMed Inc.
K212500	08/09/2021	ArtiSential Trocar	LivsMed Inc.
K203580	12/07/2020	ArtiSential Laparoscopic Instruments-Electrodes	LivsMed Inc.
K230498	02/24/2023	ArtiSential Laparoscopic Instruments-Electrodes	LivsMed Inc.
K230499	02/24/2023	ArtiSential Laparoscopic Instruments-Electrodes	LivsMed Inc.
K230539	02/27/2023	ArtiSential Laparoscopic Instruments-Electrodes	LivsMed Inc.
K200501	02/28/2020	ArtiSential Laparoscopic Instrument-Electrodes	LivsMed Inc.
K190909	04/08/2019	ArtiSential Bipolar Fenestrated Forceps	Livsmed Inc.
K241138	04/24/2024	ArtiSeal Vessel Sealing System-ArtiSeal Instruments; ArtiSeal Vessel Sealing System-ArtiSeal Generator	LivsMed Inc.
K240657	03/08/2024	ArtiSential Laparoscopic Instruments-Electrodes (AMHD01-LH); ArtiSential Laparoscopic Instruments-Electrodes (AMHD01S-LH); ArtiSential Laparoscopic Instruments-Electrodes (AMHD01L-LH); ArtiSential Laparoscopic Instruments-Electrodes (5AMHD01-LH); ArtiSent	LivsMed Inc.