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FDA 510(k)

Epix Electrosurgical Probe with Smoke Evacuation

K-Number: K151480 · 2016-02-19

ApplicantApplied Medical Resources
Decision Date2016-02-19
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Epix Electrosurgical Probe with Smoke Evacuation is a medical device manufactured by Applied Medical Resources. It received FDA 510(k) clearance on 2016-02-19 under approval number K151480. 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 2016-02-19. It is manufactured by Applied Medical Resources. The 510(k) number is K151480.

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

Epix Electrosurgical Probe with Smoke Evacuation received FDA 510(k) clearance on 2016-02-19, under approval number K151480.

What company makes Epix Electrosurgical Probe with Smoke Evacuation?

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

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

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