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FDA 510(k)

General Cutting Contra Handpiece

K-Number: K182999 · 2019-04-16

ApplicantNakanishi, Inc.
Decision Date2019-04-16
Product CodeEGS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

General Cutting Contra Handpiece is a medical device manufactured by Nakanishi, Inc.. It received FDA 510(k) clearance on 2019-04-16 under approval number K182999. The device is classified under product code EGS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the General Cutting Contra Handpiece?

General Cutting Contra Handpiece is a medical device that received FDA 510(k) clearance on 2019-04-16. It is manufactured by Nakanishi, Inc.. The 510(k) number is K182999.

When was General Cutting Contra Handpiece approved by the FDA?

General Cutting Contra Handpiece received FDA 510(k) clearance on 2019-04-16, under approval number K182999.

What company makes General Cutting Contra Handpiece?

General Cutting Contra Handpiece is manufactured by Nakanishi, Inc..

What is the FDA product code for General Cutting Contra Handpiece?

The FDA product code for General Cutting Contra Handpiece is EGS.

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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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