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FDA 510(k)

General Cutting Straight

K-Number: K230106 · 2023-05-24

ApplicantNakanishi, Inc.
Decision Date2023-05-24
Product CodeEGS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

General Cutting Straight is the device name listed in this FDA 510(k) record. The listed applicant is Nakanishi, Inc.. It received FDA 510(k) clearance on 2023-05-24 under 510(k) number K230106. 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 Straight?

General Cutting Straight is a medical device that received FDA 510(k) clearance on 2023-05-24. The listed applicant is Nakanishi, Inc.. The 510(k) number is K230106.

When did General Cutting Straight receive FDA 510(k) clearance?

General Cutting Straight received FDA 510(k) clearance on 2023-05-24, under 510(k) number K230106.

Who is the listed applicant for General Cutting Straight?

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

What is the FDA product code for General Cutting Straight?

The FDA product code for General Cutting Straight 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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