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FDA 510(k)

Voyant Electrosurgical Generator

K-Number: K182244 · 2018-10-11

ApplicantApplied Medical Resources Corp.
Decision Date2018-10-11
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Voyant Electrosurgical Generator is a medical device manufactured by Applied Medical Resources Corp.. It received FDA 510(k) clearance on 2018-10-11 under approval number K182244. 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 Voyant Electrosurgical Generator?

Voyant Electrosurgical Generator is a medical device that received FDA 510(k) clearance on 2018-10-11. It is manufactured by Applied Medical Resources Corp.. The 510(k) number is K182244.

When was Voyant Electrosurgical Generator approved by the FDA?

Voyant Electrosurgical Generator received FDA 510(k) clearance on 2018-10-11, under approval number K182244.

What company makes Voyant Electrosurgical Generator?

Voyant Electrosurgical Generator is manufactured by Applied Medical Resources Corp..

What is the FDA product code for Voyant Electrosurgical Generator?

The FDA product code for Voyant Electrosurgical Generator is GEI.

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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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