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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Livsmed, Inc.. It received FDA 510(k) clearance on 2020-06-17 under 510(k) 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. The listed applicant is Livsmed, Inc.. The 510(k) number is K200875.

When did ArtiSential Laparoscopic Instruments - Electrodes receive FDA 510(k) clearance?

ArtiSential Laparoscopic Instruments - Electrodes received FDA 510(k) clearance on 2020-06-17, under 510(k) number K200875.

Who is the listed applicant for ArtiSential Laparoscopic Instruments - Electrodes?

The FDA 510(k) record lists Livsmed, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ArtiSential Laparoscopic Instruments - Electrodes?

The FDA product code for ArtiSential Laparoscopic Instruments - Electrodes is GEI.

Other records listing Livsmed, Inc. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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