ArtiSential Laparoscopic Instruments - Electrodes
K-Number: K200875 · 2020-06-17
ApplicantLivsmed, Inc.
Decision Date2020-06-17
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 2020-06-17 under approval number K200875. 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 2020-06-17. It is manufactured by Livsmed, Inc.. The 510(k) number is K200875.
When was ArtiSential Laparoscopic Instruments - Electrodes approved by the FDA?
ArtiSential Laparoscopic Instruments - Electrodes received FDA 510(k) clearance on 2020-06-17, under approval number K200875.
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.