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FDA 510(k)

Cut-Vac Lighted Smoke Evacuation Electrosurgical Pencil

K-Number: K170721 · 2017-04-21

ApplicantPrecision Surgical, LLC
Decision Date2017-04-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Cut-Vac Lighted Smoke Evacuation Electrosurgical Pencil is a medical device manufactured by Precision Surgical, LLC. It received FDA 510(k) clearance on 2017-04-21 under approval number K170721. 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 Cut-Vac Lighted Smoke Evacuation Electrosurgical Pencil?

Cut-Vac Lighted Smoke Evacuation Electrosurgical Pencil is a medical device that received FDA 510(k) clearance on 2017-04-21. It is manufactured by Precision Surgical, LLC. The 510(k) number is K170721.

When was Cut-Vac Lighted Smoke Evacuation Electrosurgical Pencil approved by the FDA?

Cut-Vac Lighted Smoke Evacuation Electrosurgical Pencil received FDA 510(k) clearance on 2017-04-21, under approval number K170721.

What company makes Cut-Vac Lighted Smoke Evacuation Electrosurgical Pencil?

Cut-Vac Lighted Smoke Evacuation Electrosurgical Pencil is manufactured by Precision Surgical, LLC.

What is the FDA product code for Cut-Vac Lighted Smoke Evacuation Electrosurgical Pencil?

The FDA product code for Cut-Vac Lighted Smoke Evacuation Electrosurgical Pencil 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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