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FDA 510(k)

Fujifilm Diathermic Slitter (FlushKnife)

K-Number: K171096 · 2017-05-09

ApplicantFujifilm Medical Systems U.S.A, Inc.
Decision Date2017-05-09
Product CodeKGE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Fujifilm Diathermic Slitter (FlushKnife) is the device name listed in this FDA 510(k) record. The listed applicant is Fujifilm Medical Systems U.S.A, Inc.. It received FDA 510(k) clearance on 2017-05-09 under 510(k) number K171096. The device is classified under product code KGE. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Fujifilm Diathermic Slitter (FlushKnife)?

Fujifilm Diathermic Slitter (FlushKnife) is a medical device that received FDA 510(k) clearance on 2017-05-09. The listed applicant is Fujifilm Medical Systems U.S.A, Inc.. The 510(k) number is K171096.

When did Fujifilm Diathermic Slitter (FlushKnife) receive FDA 510(k) clearance?

Fujifilm Diathermic Slitter (FlushKnife) received FDA 510(k) clearance on 2017-05-09, under 510(k) number K171096.

Who is the listed applicant for Fujifilm Diathermic Slitter (FlushKnife)?

The FDA 510(k) record lists Fujifilm Medical Systems U.S.A, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Fujifilm Diathermic Slitter (FlushKnife)?

The FDA product code for Fujifilm Diathermic Slitter (FlushKnife) is KGE.

Other records listing Fujifilm Medical Systems U.S.A, Inc. as applicant

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Related Devices (Code: KGE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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