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FDA 510(k)

Epix Electrosurgical Probe with Smoke Evacuation

K-Number: K171684 · 2017-08-07

ApplicantApplied Medical Resources Corporation
Decision Date2017-08-07
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Epix Electrosurgical Probe with Smoke Evacuation is a medical device manufactured by Applied Medical Resources Corporation. It received FDA 510(k) clearance on 2017-08-07 under approval number K171684. 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 Epix Electrosurgical Probe with Smoke Evacuation?

Epix Electrosurgical Probe with Smoke Evacuation is a medical device that received FDA 510(k) clearance on 2017-08-07. It is manufactured by Applied Medical Resources Corporation. The 510(k) number is K171684.

When was Epix Electrosurgical Probe with Smoke Evacuation approved by the FDA?

Epix Electrosurgical Probe with Smoke Evacuation received FDA 510(k) clearance on 2017-08-07, under approval number K171684.

What company makes Epix Electrosurgical Probe with Smoke Evacuation?

Epix Electrosurgical Probe with Smoke Evacuation is manufactured by Applied Medical Resources Corporation.

What is the FDA product code for Epix Electrosurgical Probe with Smoke Evacuation?

The FDA product code for Epix Electrosurgical Probe with Smoke Evacuation 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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