FDA 510(k)

Codman Electrosurgical Generator, Foot Pedal

K-Number: K183526 · 2019-04-11

Decision Date2019-04-11

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

Codman Electrosurgical Generator, Foot Pedal is a medical device manufactured by Kls Martin GmbH + Co. KG. It received FDA 510(k) clearance on 2019-04-11 under approval number K183526. 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 Codman Electrosurgical Generator, Foot Pedal?

Codman Electrosurgical Generator, Foot Pedal is a medical device that received FDA 510(k) clearance on 2019-04-11. It is manufactured by Kls Martin GmbH + Co. KG. The 510(k) number is K183526.

When was Codman Electrosurgical Generator, Foot Pedal approved by the FDA?

Codman Electrosurgical Generator, Foot Pedal received FDA 510(k) clearance on 2019-04-11, under approval number K183526.

What company makes Codman Electrosurgical Generator, Foot Pedal?

Codman Electrosurgical Generator, Foot Pedal is manufactured by Kls Martin GmbH + Co. KG.

What is the FDA product code for Codman Electrosurgical Generator, Foot Pedal?

The FDA product code for Codman Electrosurgical Generator, Foot Pedal is GEI.

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Official Source

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