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FDA 510(k)

ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340)

K-Number: K234033 · 2024-05-06

ApplicantBoehringer Laboratories, LLC
Decision Date2024-05-06
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340) is a medical device manufactured by Boehringer Laboratories, LLC. It received FDA 510(k) clearance on 2024-05-06 under approval number K234033. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340)?

ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340) is a medical device that received FDA 510(k) clearance on 2024-05-06. It is manufactured by Boehringer Laboratories, LLC. The 510(k) number is K234033.

When was ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340) approved by the FDA?

ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340) received FDA 510(k) clearance on 2024-05-06, under approval number K234033.

What company makes ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340)?

ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340) is manufactured by Boehringer Laboratories, LLC.

What is the FDA product code for ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340)?

The FDA product code for ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340) is KNT.

Other Devices by Boehringer Laboratories, LLC

K243399Boehringer Laboratories Liver Retractor

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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.

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