FDA 510(k)

LUDWIG Electrosurgical Device

K-Number: K221574 · 2022-10-16

Decision Date2022-10-16

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

LUDWIG Electrosurgical Device is a medical device manufactured by Aesthetics Biomedical. It received FDA 510(k) clearance on 2022-10-16 under approval number K221574. 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 LUDWIG Electrosurgical Device?

LUDWIG Electrosurgical Device is a medical device that received FDA 510(k) clearance on 2022-10-16. It is manufactured by Aesthetics Biomedical. The 510(k) number is K221574.

When was LUDWIG Electrosurgical Device approved by the FDA?

LUDWIG Electrosurgical Device received FDA 510(k) clearance on 2022-10-16, under approval number K221574.

What company makes LUDWIG Electrosurgical Device?

LUDWIG Electrosurgical Device is manufactured by Aesthetics Biomedical.

What is the FDA product code for LUDWIG Electrosurgical Device?

The FDA product code for LUDWIG Electrosurgical Device is GEI.

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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.