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FDA 510(k)

TOPKIN WOUND DRESSING

K-Number: K031684 · 2003-10-30

ApplicantBiomet Merck GmbH
Decision Date2003-10-30
Product CodeQSZ
DecisionSubstantially Equivalent

Device Summary

TOPKIN WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Merck GmbH. It received FDA 510(k) clearance on 2003-10-30 under 510(k) number K031684. The device is classified under product code QSZ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOPKIN WOUND DRESSING?

TOPKIN WOUND DRESSING is a medical device that received FDA 510(k) clearance on 2003-10-30. The listed applicant is Biomet Merck GmbH. The 510(k) number is K031684.

When did TOPKIN WOUND DRESSING receive FDA 510(k) clearance?

TOPKIN WOUND DRESSING received FDA 510(k) clearance on 2003-10-30, under 510(k) number K031684.

Who is the listed applicant for TOPKIN WOUND DRESSING?

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

What is the FDA product code for TOPKIN WOUND DRESSING?

The FDA product code for TOPKIN WOUND DRESSING is QSZ.

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Related Devices (Code: QSZ)

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.

K261311HYALOMATRIXAnika Therapeutics, Inc.K254256LUOFUCON® Wound MatrixHuizhou Foryou Medical Devices Co., Ltd.K260020Redermo Wound MatrixBeijing Kreate Medical Co., Ltd.K251567NovoSorb BTMPolynovo Biomaterials Pty, Ltd.K242149NovoSorb® MTXPolynovo Biomaterials Pty, Ltd.K241660SiOxD® Wound MatrixSioxmed, LLC

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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