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FDA 510(k)

Codman Electrosurgical Generator, Foot Pedal

K-Number: K183526 · 2019-04-11

ApplicantKls Martin GmbH + Co. KG
Decision Date2019-04-11
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Codman Electrosurgical Generator, Foot Pedal is the device name listed in this FDA 510(k) record. The listed applicant is Kls Martin GmbH + Co. KG. It received FDA 510(k) clearance on 2019-04-11 under 510(k) 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. The listed applicant is Kls Martin GmbH + Co. KG. The 510(k) number is K183526.

When did Codman Electrosurgical Generator, Foot Pedal receive FDA 510(k) clearance?

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

Who is the listed applicant for Codman Electrosurgical Generator, Foot Pedal?

The FDA 510(k) record lists Kls Martin GmbH + Co. KG as the applicant. This does not by itself establish the device manufacturer.

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

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