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FDA 510(k)

CURAD SILVER ACTIVE GEL BANDAGE

K-Number: K032462 · 2004-02-10

ApplicantBeiersdorf AG
Decision Date2004-02-10
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

CURAD SILVER ACTIVE GEL BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is Beiersdorf AG. It received FDA 510(k) clearance on 2004-02-10 under 510(k) number K032462. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURAD SILVER ACTIVE GEL BANDAGE?

CURAD SILVER ACTIVE GEL BANDAGE is a medical device that received FDA 510(k) clearance on 2004-02-10. The listed applicant is Beiersdorf AG. The 510(k) number is K032462.

When did CURAD SILVER ACTIVE GEL BANDAGE receive FDA 510(k) clearance?

CURAD SILVER ACTIVE GEL BANDAGE received FDA 510(k) clearance on 2004-02-10, under 510(k) number K032462.

Who is the listed applicant for CURAD SILVER ACTIVE GEL BANDAGE?

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

What is the FDA product code for CURAD SILVER ACTIVE GEL BANDAGE?

The FDA product code for CURAD SILVER ACTIVE GEL BANDAGE is FRO. This falls under the Anesthesiology category.

Related Clinical Trials

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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Other records listing Beiersdorf AG as applicant

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.

K032463CURAD SILVER BANDAGEK022645CURAD

Related Devices (Code: FRO)

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.

K254168Actolind® (06.3637. Actolind® Gel Plus)ACTO GmbHK254041SkinSmart Antimicrobial HydroGelMagic Science Supply, LLCK261646Redermax® Antibacterial Wound MatrixBeijing Kreate Medical Co., Ltd.K253665Vashe Plus Antimicrobial SolutionUrgo Medical North America, LLCK251929SilverCeuticals® Antimicrobial Wound GelSilverceuticals, Inc.K261023Microdacyn Wound Irrigation SolutionSonoma Pharmaceuticals, Inc.

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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