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FDA 510(k)

GIRAFFE2

K-Number: K102133 · 2010-10-07

ApplicantKerr Corporation
Decision Date2010-10-07
Product CodeMVL
DecisionSubstantially Equivalent

Device Summary

GIRAFFE2 is the device name listed in this FDA 510(k) record. The listed applicant is Kerr Corporation. It received FDA 510(k) clearance on 2010-10-07 under 510(k) number K102133. The device is classified under product code MVL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GIRAFFE2?

GIRAFFE2 is a medical device that received FDA 510(k) clearance on 2010-10-07. The listed applicant is Kerr Corporation. The 510(k) number is K102133.

When did GIRAFFE2 receive FDA 510(k) clearance?

GIRAFFE2 received FDA 510(k) clearance on 2010-10-07, under 510(k) number K102133.

Who is the listed applicant for GIRAFFE2?

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

What is the FDA product code for GIRAFFE2?

The FDA product code for GIRAFFE2 is MVL.

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Other records listing Kerr Corporation as applicant

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Related Devices (Code: MVL)

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.

K254239CyClean CordSS GLOBALK253797One-StopMediclus Co., Ltd.K243910RetraxilKulzer, LLCK211420Stasis GelBelport Company, Inc., Gingi-PakK211419Gingi-Aid GelBelport Company, Inc., Gingi-PakK213149VOCO Retraction PasteVoco GmbH

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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