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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 the device name listed in this FDA 510(k) record. The listed applicant is Precision Surgical, LLC. It received FDA 510(k) clearance on 2017-04-21 under 510(k) 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. The listed applicant is Precision Surgical, LLC. The 510(k) number is K170721.

When did Cut-Vac Lighted Smoke Evacuation Electrosurgical Pencil receive FDA 510(k) clearance?

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

Who is the listed applicant for Cut-Vac Lighted Smoke Evacuation Electrosurgical Pencil?

The FDA 510(k) record lists Precision Surgical, LLC as the applicant. This does not by itself establish the device manufacturer.

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

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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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