ArtiSential Laparoscopic Instruments-Electrodes
K-Number: K230539 · 2023-04-27
ApplicantLivsmed, Inc.
Decision Date2023-04-27
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
ArtiSential Laparoscopic Instruments-Electrodes is a medical device manufactured by Livsmed, Inc.. It received FDA 510(k) clearance on 2023-04-27 under approval number K230539. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ArtiSential Laparoscopic Instruments-Electrodes?
ArtiSential Laparoscopic Instruments-Electrodes is a medical device that received FDA 510(k) clearance on 2023-04-27. It is manufactured by Livsmed, Inc.. The 510(k) number is K230539.
When was ArtiSential Laparoscopic Instruments-Electrodes approved by the FDA?
ArtiSential Laparoscopic Instruments-Electrodes received FDA 510(k) clearance on 2023-04-27, under approval number K230539.
What company makes ArtiSential Laparoscopic Instruments-Electrodes?
ArtiSential Laparoscopic Instruments-Electrodes is manufactured by Livsmed, Inc..
What is the FDA product code for ArtiSential Laparoscopic Instruments-Electrodes?
The FDA product code for ArtiSential Laparoscopic Instruments-Electrodes is GEI.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.